Canonical Allele Identifier: CA2991011067
Gene: MUTYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332227dup , CM000663.2:g.45332227dup GRCh38
NC_000001.10:g.45797899dup , CM000663.1:g.45797899dup GRCh37
NC_000001.9:g.45570486dup NCBI36
NG_008189.1:g.13247dup , LRG_220:g.13247dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.407dup ENSP00000410263.2:p.Gln137ThrfsTer?
ENST00000435155.2:c.824dup ENSP00000403655.2:p.Gln276ThrfsTer?
ENST00000467459.6:c.791dup ENSP00000435889.2:p.Gln265ThrfsTer?
ENST00000483127.2:c.809dup ENSP00000436469.2:p.Gln271ThrfsTer?
ENST00000485271.6:c.791dup ENSP00000431264.2:p.Gln265ThrfsTer?
ENST00000529892.6:c.833dup ENSP00000432528.2:p.Gln279ThrfsTer?
ENST00000533178.6:c.*120dup ENSP00000436430.2:n.*120dup
ENST00000672314.2:c.791dup ENSP00000500828.2:p.Gln265ThrfsTer?
ENST00000674679.2:c.*703dup ENSP00000501623.2:n.*703dup
ENST00000710952.2:c.875dup MANE Plus Clinical ENSP00000518552.2:p.Gln293ThrfsTer?
ENST00000672818.3:c.866dup ENSP00000500891.1:p.Gln290ThrfsTer?
ENST00000450313.6:c.*120dup ENSP00000408176.2:n.*120dup
ENST00000456914.7:c.791dup MANE Select ENSP00000407590.2:p.Gln265ThrfsTer?
ENST00000461495.6:c.*530dup ENSP00000437166.1:n.*530dup
ENST00000671898.1:c.1379dup ENSP00000499896.1:p.Gln461ThrfsTer?
ENST00000672011.1:c.*120dup ENSP00000500418.1:n.*120dup
ENST00000672314.1:c.791dup ENSP00000500828.1:p.Gln265ThrfsTer?
ENST00000672593.1:c.*844dup ENSP00000500455.1:n.*844dup
ENST00000672764.1:c.*120dup ENSP00000500886.1:n.*120dup
ENST00000672818.2:c.866dup ENSP00000500891.1:p.Gln290ThrfsTer?
ENST00000673134.1:c.*488dup ENSP00000500526.1:n.*488dup
ENST00000674679.1:c.819dup ENSP00000501623.1:n.819dup
ENST00000354383.10:c.794dup ENSP00000346354.6:p.Gln266ThrfsTer?
ENST00000355498.6:c.791dup ENSP00000347685.2:p.Gln265ThrfsTer?
ENST00000372098.7:c.866dup ENSP00000361170.3:p.Gln290ThrfsTer?
ENST00000372104.5:c.791dup ENSP00000361176.1:p.Gln265ThrfsTer?
ENST00000372110.7:c.836dup ENSP00000361182.3:p.Gln280ThrfsTer?
ENST00000372115.7:c.833dup ENSP00000361187.3:p.Gln279ThrfsTer?
ENST00000412971.5:c.407dup ENSP00000410263.1:p.Gln137ThrfsTer?
ENST00000435155.1:c.824dup ENSP00000403655.1:p.Gln276ThrfsTer?
ENST00000448481.5:c.824dup ENSP00000409718.1:p.Gln276ThrfsTer?
ENST00000450313.5:c.875dup ENSP00000408176.1:p.Gln293ThrfsTer?
ENST00000456914.6:c.791dup ENSP00000407590.2:p.Gln265ThrfsTer?
ENST00000461495.5:c.*530dup ENSP00000437166.1:n.*530dup
ENST00000462388.5:n.482dup
ENST00000466231.1:n.156dup
ENST00000467459.5:c.185dup ENSP00000435889.1:p.Gln63ThrfsTer?
ENST00000467940.5:c.*714dup ENSP00000436478.1:n.*714dup
ENST00000470256.5:c.*120dup ENSP00000434985.1:n.*120dup
ENST00000475516.5:c.*604dup ENSP00000433843.1:n.*604dup
ENST00000478796.5:n.778dup
ENST00000481571.5:c.*604dup ENSP00000436597.1:n.*604dup
ENST00000488731.6:c.187+539dup ENSP00000432330.1:n.187+539dup
ENST00000528013.6:c.833dup ENSP00000433130.2:p.Gln279ThrfsTer?
ENST00000529892.5:c.55dup
ENST00000529984.5:c.187+539dup ENSP00000437093.1:n.187+539dup
ENST00000531105.5:c.115+2167dup ENSP00000431292.1:n.115+2167dup
ENST00000533178.5:c.420dup ENSP00000436430.1:n.420dup
NM_001048171.1:c.833dup NP_001041636.1:p.Gln279ThrfsTer?
NM_001048172.1:c.794dup NP_001041637.1:p.Gln266ThrfsTer?
NM_001048173.1:c.791dup NP_001041638.1:p.Gln265ThrfsTer?
NM_001048174.1:c.791dup NP_001041639.1:p.Gln265ThrfsTer?
NM_001128425.1:c.875dup , LRG_220t1:c.875dup NP_001121897.1:p.Gln293ThrfsTer?
NM_001293190.1:c.836dup NP_001280119.1:p.Gln280ThrfsTer?
NM_001293191.1:c.824dup NP_001280120.1:p.Gln276ThrfsTer?
NM_001293192.1:c.515dup NP_001280121.1:p.Gln173ThrfsTer?
NM_001293195.1:c.791dup NP_001280124.1:p.Gln265ThrfsTer?
NM_001293196.1:c.515dup NP_001280125.1:p.Gln173ThrfsTer?
NM_012222.2:c.866dup NP_036354.1:p.Gln290ThrfsTer?
XM_011541497.1:c.851dup XP_011539799.1:p.Gln285ThrfsTer?
XM_011541498.1:c.833dup XP_011539800.1:p.Gln279ThrfsTer?
XM_011541499.1:c.833dup XP_011539801.1:p.Gln279ThrfsTer?
XM_011541500.1:c.833dup XP_011539802.1:p.Gln279ThrfsTer?
XM_011541501.1:c.833dup XP_011539803.1:p.Gln279ThrfsTer?
XM_011541502.1:c.833dup XP_011539804.1:p.Gln279ThrfsTer?
XM_011541503.1:c.833dup XP_011539805.1:p.Gln279ThrfsTer?
XM_011541504.1:c.824dup XP_011539806.1:p.Gln276ThrfsTer?
XM_011541505.1:c.413dup XP_011539807.1:p.Gln139ThrfsTer?
XM_011541506.1:c.413dup XP_011539808.1:p.Gln139ThrfsTer?
XM_011541507.1:c.404dup XP_011539809.1:p.Gln136ThrfsTer?
XM_011541508.1:c.419dup XP_011539810.1:p.Gln141ThrfsTer?
XR_946658.1:n.922dup
NM_001350650.1:c.446dup NP_001337579.1:p.Gln150ThrfsTer?
NM_001350651.1:c.446dup NP_001337580.1:p.Gln150ThrfsTer?
NR_146882.1:n.1049dup
NR_146883.1:n.863dup
XM_011541497.3:c.851dup XP_011539799.1:p.Gln285ThrfsTer?
XM_011541500.3:c.833dup XP_011539802.1:p.Gln279ThrfsTer?
XM_011541501.2:c.833dup XP_011539803.1:p.Gln279ThrfsTer?
XM_011541502.2:c.833dup XP_011539804.1:p.Gln279ThrfsTer?
XM_011541503.2:c.833dup XP_011539805.1:p.Gln279ThrfsTer?
XM_011541504.2:c.824dup XP_011539806.1:p.Gln276ThrfsTer?
XM_011541505.2:c.413dup XP_011539807.1:p.Gln139ThrfsTer?
XM_011541506.2:c.413dup XP_011539808.1:p.Gln139ThrfsTer?
XM_017001331.1:c.833dup XP_016856820.1:p.Gln279ThrfsTer?
XM_017001332.1:c.833dup XP_016856821.1:p.Gln279ThrfsTer?
XM_017001333.1:c.833dup XP_016856822.1:p.Gln279ThrfsTer?
XM_017001334.1:c.794dup XP_016856823.1:p.Gln266ThrfsTer?
XM_017001335.1:c.515dup XP_016856824.1:p.Gln173ThrfsTer?
XM_017001336.1:c.446dup XP_016856825.1:p.Gln150ThrfsTer?
XM_017001337.1:c.446dup XP_016856826.1:p.Gln150ThrfsTer?
XM_024447244.1:c.446dup XP_024303012.1:p.Gln150ThrfsTer?
XM_024447245.1:c.446dup XP_024303013.1:p.Gln150ThrfsTer?
XM_024447248.1:c.404dup XP_024303016.1:p.Gln136ThrfsTer?
XM_024447249.1:c.275dup XP_024303017.1:p.Gln93ThrfsTer?
XM_024447250.1:c.275dup XP_024303018.1:p.Gln93ThrfsTer?
XM_024447251.1:c.275dup XP_024303019.1:p.Gln93ThrfsTer?
XR_001737190.1:n.836dup
XR_001737192.1:n.648dup
XR_002956643.1:n.828dup
XR_002956644.1:n.1363dup
XR_946658.2:n.936dup
NM_001048171.2:c.791dup NP_001041636.2:p.Gln265ThrfsTer?
NM_001128425.2:c.875dup MANE Plus Clinical NP_001121897.1:p.Gln293ThrfsTer?
NM_001048172.2:c.794dup NP_001041637.1:p.Gln266ThrfsTer?
NM_001048173.2:c.791dup NP_001041638.1:p.Gln265ThrfsTer?
NM_001048174.2:c.791dup MANE Select NP_001041639.1:p.Gln265ThrfsTer?
NM_001293190.2:c.836dup NP_001280119.1:p.Gln280ThrfsTer?
NM_001293191.2:c.824dup NP_001280120.1:p.Gln276ThrfsTer?
NM_001293192.2:c.515dup NP_001280121.1:p.Gln173ThrfsTer?
NM_001293195.2:c.791dup NP_001280124.1:p.Gln265ThrfsTer?
NM_001293196.2:c.515dup NP_001280125.1:p.Gln173ThrfsTer?
NM_001350650.2:c.446dup NP_001337579.1:p.Gln150ThrfsTer?
NM_001350651.2:c.446dup NP_001337580.1:p.Gln150ThrfsTer?
NM_012222.3:c.866dup NP_036354.1:p.Gln290ThrfsTer?
NR_146882.2:n.1019dup
NR_146883.2:n.868dup