Canonical Allele Identifier: CA2573132097
Gene: MUTYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45333111dup , CM000663.2:g.45333111dup GRCh38
NC_000001.10:g.45798783dup , CM000663.1:g.45798783dup GRCh37
NC_000001.9:g.45571370dup NCBI36
NG_008189.1:g.12360dup , LRG_220:g.12360dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.37-277dup ENSP00000410263.2:n.37-277dup
ENST00000435155.2:c.397dup ENSP00000403655.2:p.Thr133AsnfsTer?
ENST00000467459.6:c.364dup ENSP00000435889.2:p.Thr122AsnfsTer?
ENST00000483127.2:c.382dup ENSP00000436469.2:p.Thr128AsnfsTer?
ENST00000485271.6:c.364dup ENSP00000431264.2:p.Thr122AsnfsTer?
ENST00000529892.6:c.406dup ENSP00000432528.2:p.Thr136AsnfsTer?
ENST00000533178.6:c.116-424dup ENSP00000436430.2:n.116-424dup
ENST00000672314.2:c.364dup ENSP00000500828.2:p.Thr122AsnfsTer?
ENST00000674679.2:c.*276dup ENSP00000501623.2:n.*276dup
ENST00000710952.2:c.448dup MANE Plus Clinical ENSP00000518552.2:p.Thr150AsnfsTer?
ENST00000672818.3:c.439dup ENSP00000500891.1:p.Thr147AsnfsTer?
ENST00000450313.6:c.389-152dup ENSP00000408176.2:n.389-152dup
ENST00000456914.7:c.364dup MANE Select ENSP00000407590.2:p.Thr122AsnfsTer?
ENST00000461495.6:c.*118-152dup ENSP00000437166.1:n.*118-152dup
ENST00000671856.1:n.325-152dup
ENST00000671898.1:c.952dup ENSP00000499896.1:p.Thr318AsnfsTer?
ENST00000672011.1:c.347-152dup ENSP00000500418.1:n.347-152dup
ENST00000672314.1:c.364dup ENSP00000500828.1:p.Thr122AsnfsTer?
ENST00000672593.1:c.*177dup ENSP00000500455.1:n.*177dup
ENST00000672764.1:c.338-152dup ENSP00000500886.1:n.338-152dup
ENST00000672818.2:c.439dup ENSP00000500891.1:p.Thr147AsnfsTer?
ENST00000673134.1:c.*117+174dup ENSP00000500526.1:n.*117+174dup
ENST00000674679.1:c.392dup ENSP00000501623.1:n.392dup
ENST00000354383.10:c.367dup ENSP00000346354.6:p.Thr123AsnfsTer?
ENST00000355498.6:c.364dup ENSP00000347685.2:p.Thr122AsnfsTer?
ENST00000372098.7:c.439dup ENSP00000361170.3:p.Thr147AsnfsTer?
ENST00000372104.5:c.364dup ENSP00000361176.1:p.Thr122AsnfsTer?
ENST00000372110.7:c.409dup ENSP00000361182.3:p.Thr137AsnfsTer?
ENST00000372115.7:c.406dup ENSP00000361187.3:p.Thr136AsnfsTer?
ENST00000412971.5:c.37-277dup ENSP00000410263.1:n.37-277dup
ENST00000435155.1:c.397dup ENSP00000403655.1:p.Thr133AsnfsTer?
ENST00000448481.5:c.397dup ENSP00000409718.1:p.Thr133AsnfsTer?
ENST00000450313.5:c.448dup ENSP00000408176.1:p.Thr150AsnfsTer?
ENST00000456914.6:c.364dup ENSP00000407590.2:p.Thr122AsnfsTer?
ENST00000461495.5:c.*118-152dup ENSP00000437166.1:n.*118-152dup
ENST00000462387.5:n.549dup
ENST00000467940.5:c.*287dup ENSP00000436478.1:n.*287dup
ENST00000470256.5:c.307+174dup ENSP00000434985.1:n.307+174dup
ENST00000474703.1:n.519dup
ENST00000475516.5:c.*177dup ENSP00000433843.1:n.*177dup
ENST00000476789.5:n.584dup
ENST00000478796.5:n.214dup
ENST00000479746.6:n.427dup
ENST00000481139.5:n.617dup
ENST00000481571.5:c.*177dup ENSP00000436597.1:n.*177dup
ENST00000483642.5:n.659dup
ENST00000485484.5:n.528dup
ENST00000488731.6:c.116-277dup ENSP00000432330.1:n.116-277dup
ENST00000492494.5:n.541dup
ENST00000525160.5:c.*30-152dup ENSP00000431568.1:n.*30-152dup
ENST00000528013.6:c.406dup ENSP00000433130.2:p.Thr136AsnfsTer?
ENST00000529984.5:c.116-277dup ENSP00000437093.1:n.116-277dup
ENST00000531105.5:c.115+1280dup ENSP00000431292.1:n.115+1280dup
ENST00000533178.5:c.122-424dup ENSP00000436430.1:n.122-424dup
NM_001048171.1:c.406dup NP_001041636.1:p.Thr136AsnfsTer?
NM_001048172.1:c.367dup NP_001041637.1:p.Thr123AsnfsTer?
NM_001048173.1:c.364dup NP_001041638.1:p.Thr122AsnfsTer?
NM_001048174.1:c.364dup NP_001041639.1:p.Thr122AsnfsTer?
NM_001128425.1:c.448dup , LRG_220t1:c.448dup NP_001121897.1:p.Thr150AsnfsTer?
NM_001293190.1:c.409dup NP_001280119.1:p.Thr137AsnfsTer?
NM_001293191.1:c.397dup NP_001280120.1:p.Thr133AsnfsTer?
NM_001293192.1:c.88dup NP_001280121.1:p.Thr30AsnfsTer?
NM_001293195.1:c.364dup NP_001280124.1:p.Thr122AsnfsTer?
NM_001293196.1:c.88dup NP_001280125.1:p.Thr30AsnfsTer?
NM_012222.2:c.439dup NP_036354.1:p.Thr147AsnfsTer?
XM_011541497.1:c.424dup XP_011539799.1:p.Thr142AsnfsTer?
XM_011541498.1:c.406dup XP_011539800.1:p.Thr136AsnfsTer?
XM_011541499.1:c.406dup XP_011539801.1:p.Thr136AsnfsTer?
XM_011541500.1:c.406dup XP_011539802.1:p.Thr136AsnfsTer?
XM_011541501.1:c.406dup XP_011539803.1:p.Thr136AsnfsTer?
XM_011541502.1:c.406dup XP_011539804.1:p.Thr136AsnfsTer?
XM_011541503.1:c.448dup XP_011539805.1:p.Thr150AsnfsTer?
XM_011541504.1:c.397dup XP_011539806.1:p.Thr133AsnfsTer?
XM_011541505.1:c.43-277dup XP_011539807.1:n.43-277dup
XM_011541506.1:c.43-277dup XP_011539808.1:n.43-277dup
XM_011541507.1:c.33+174dup XP_011539809.1:n.33+174dup
XM_011541508.1:c.7-152dup XP_011539810.1:n.7-152dup
XR_946658.1:n.495dup
NM_001350650.1:c.34-152dup NP_001337579.1:n.34-152dup
NM_001350651.1:c.34-152dup NP_001337580.1:n.34-152dup
NR_146882.1:n.622dup
NR_146883.1:n.451-152dup
XM_011541497.3:c.424dup XP_011539799.1:p.Thr142AsnfsTer?
XM_011541500.3:c.406dup XP_011539802.1:p.Thr136AsnfsTer?
XM_011541501.2:c.406dup XP_011539803.1:p.Thr136AsnfsTer?
XM_011541502.2:c.406dup XP_011539804.1:p.Thr136AsnfsTer?
XM_011541503.2:c.448dup XP_011539805.1:p.Thr150AsnfsTer?
XM_011541504.2:c.397dup XP_011539806.1:p.Thr133AsnfsTer?
XM_011541505.2:c.43-277dup XP_011539807.1:n.43-277dup
XM_011541506.2:c.43-277dup XP_011539808.1:n.43-277dup
XM_017001331.1:c.406dup XP_016856820.1:p.Thr136AsnfsTer?
XM_017001332.1:c.406dup XP_016856821.1:p.Thr136AsnfsTer?
XM_017001333.1:c.406dup XP_016856822.1:p.Thr136AsnfsTer?
XM_017001334.1:c.367dup XP_016856823.1:p.Thr123AsnfsTer?
XM_017001335.1:c.88dup XP_016856824.1:p.Thr30AsnfsTer?
XM_017001336.1:c.34-152dup XP_016856825.1:n.34-152dup
XM_017001337.1:c.34-152dup XP_016856826.1:n.34-152dup
XM_024447244.1:c.34-152dup XP_024303012.1:n.34-152dup
XM_024447245.1:c.34-152dup XP_024303013.1:n.34-152dup
XM_024447248.1:c.33+174dup XP_024303016.1:n.33+174dup
XM_024447249.1:c.-290dup XP_024303017.1:n.-290dup
XM_024447250.1:c.-290dup XP_024303018.1:n.-290dup
XM_024447251.1:c.-221-152dup XP_024303019.1:n.-221-152dup
XR_001737190.1:n.409dup
XR_001737192.1:n.277+174dup
XR_002956643.1:n.457+174dup
XR_002956644.1:n.716dup
XR_946658.2:n.509dup
NM_001048171.2:c.364dup NP_001041636.2:p.Thr122AsnfsTer?
NM_001128425.2:c.448dup MANE Plus Clinical NP_001121897.1:p.Thr150AsnfsTer?
NM_001048172.2:c.367dup NP_001041637.1:p.Thr123AsnfsTer?
NM_001048173.2:c.364dup NP_001041638.1:p.Thr122AsnfsTer?
NM_001048174.2:c.364dup MANE Select NP_001041639.1:p.Thr122AsnfsTer?
NM_001293190.2:c.409dup NP_001280119.1:p.Thr137AsnfsTer?
NM_001293191.2:c.397dup NP_001280120.1:p.Thr133AsnfsTer?
NM_001293192.2:c.88dup NP_001280121.1:p.Thr30AsnfsTer?
NM_001293195.2:c.364dup NP_001280124.1:p.Thr122AsnfsTer?
NM_001293196.2:c.88dup NP_001280125.1:p.Thr30AsnfsTer?
NM_001350650.2:c.34-152dup NP_001337579.1:n.34-152dup
NM_001350651.2:c.34-152dup NP_001337580.1:n.34-152dup
NM_012222.3:c.439dup NP_036354.1:p.Thr147AsnfsTer?
NR_146882.2:n.592dup
NR_146883.2:n.456-152dup