Canonical Allele Identifier: CA2991011230
Gene: MUTYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332474dup , CM000663.2:g.45332474dup GRCh38
NC_000001.10:g.45798146dup , CM000663.1:g.45798146dup GRCh37
NC_000001.9:g.45570733dup NCBI36
NG_008189.1:g.12998dup , LRG_220:g.12998dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.238dup ENSP00000410263.2:p.Asp80GlyfsTer17
ENST00000435155.2:c.655dup ENSP00000403655.2:p.Asp219GlyfsTer17
ENST00000467459.6:c.622dup ENSP00000435889.2:p.Asp208GlyfsTer17
ENST00000483127.2:c.640dup ENSP00000436469.2:p.Asp214GlyfsTer17
ENST00000485271.6:c.622dup ENSP00000431264.2:p.Asp208GlyfsTer17
ENST00000529892.6:c.664dup ENSP00000432528.2:p.Asp222GlyfsTer17
ENST00000533178.6:c.245dup ENSP00000436430.2:p.Trp83MetfsTer4
ENST00000672314.2:c.622dup ENSP00000500828.2:p.Asp208GlyfsTer17
ENST00000674679.2:c.*534dup ENSP00000501623.2:n.*534dup
ENST00000710952.2:c.706dup MANE Plus Clinical ENSP00000518552.2:p.Asp236GlyfsTer17
ENST00000672818.3:c.697dup ENSP00000500891.1:p.Asp233GlyfsTer17
ENST00000450313.6:c.632dup ENSP00000408176.2:p.Trp212MetfsTer4
ENST00000456914.7:c.622dup MANE Select ENSP00000407590.2:p.Asp208GlyfsTer17
ENST00000461495.6:c.*361dup ENSP00000437166.1:n.*361dup
ENST00000671898.1:c.1210dup ENSP00000499896.1:p.Asp404GlyfsTer17
ENST00000672011.1:c.590dup ENSP00000500418.1:p.Trp198MetfsTer4
ENST00000672314.1:c.622dup ENSP00000500828.1:p.Asp208GlyfsTer17
ENST00000672593.1:c.*595dup ENSP00000500455.1:n.*595dup
ENST00000672764.1:c.581dup ENSP00000500886.1:p.Trp195MetfsTer4
ENST00000672818.2:c.697dup ENSP00000500891.1:p.Asp233GlyfsTer17
ENST00000673134.1:c.*319dup ENSP00000500526.1:n.*319dup
ENST00000674679.1:c.650dup ENSP00000501623.1:n.650dup
ENST00000354383.10:c.625dup ENSP00000346354.6:p.Asp209GlyfsTer17
ENST00000355498.6:c.622dup ENSP00000347685.2:p.Asp208GlyfsTer17
ENST00000372098.7:c.697dup ENSP00000361170.3:p.Asp233GlyfsTer17
ENST00000372104.5:c.622dup ENSP00000361176.1:p.Asp208GlyfsTer17
ENST00000372110.7:c.667dup ENSP00000361182.3:p.Asp223GlyfsTer17
ENST00000372115.7:c.664dup ENSP00000361187.3:p.Asp222GlyfsTer17
ENST00000412971.5:c.238dup ENSP00000410263.1:p.Asp80GlyfsTer17
ENST00000435155.1:c.655dup ENSP00000403655.1:p.Asp219GlyfsTer17
ENST00000448481.5:c.655dup ENSP00000409718.1:p.Asp219GlyfsTer17
ENST00000450313.5:c.706dup ENSP00000408176.1:p.Asp236GlyfsTer17
ENST00000456914.6:c.622dup ENSP00000407590.2:p.Asp208GlyfsTer17
ENST00000461495.5:c.*361dup ENSP00000437166.1:n.*361dup
ENST00000462388.5:n.313dup
ENST00000467459.5:c.16dup ENSP00000435889.1:p.Asp6GlyfsTer17
ENST00000467940.5:c.*545dup ENSP00000436478.1:n.*545dup
ENST00000470256.5:c.509dup ENSP00000434985.1:p.Trp171MetfsTer4
ENST00000475516.5:c.*435dup ENSP00000433843.1:n.*435dup
ENST00000478796.5:n.609dup
ENST00000481571.5:c.*435dup ENSP00000436597.1:n.*435dup
ENST00000488731.6:c.187+290dup ENSP00000432330.1:n.187+290dup
ENST00000525160.5:c.*273dup ENSP00000431568.1:n.*273dup
ENST00000528013.6:c.664dup ENSP00000433130.2:p.Asp222GlyfsTer17
ENST00000529984.5:c.187+290dup ENSP00000437093.1:n.187+290dup
ENST00000531105.5:c.115+1918dup ENSP00000431292.1:n.115+1918dup
ENST00000533178.5:c.251dup ENSP00000436430.1:p.Trp85MetfsTer4
NM_001048171.1:c.664dup NP_001041636.1:p.Asp222GlyfsTer17
NM_001048172.1:c.625dup NP_001041637.1:p.Asp209GlyfsTer17
NM_001048173.1:c.622dup NP_001041638.1:p.Asp208GlyfsTer17
NM_001048174.1:c.622dup NP_001041639.1:p.Asp208GlyfsTer17
NM_001128425.1:c.706dup , LRG_220t1:c.706dup NP_001121897.1:p.Asp236GlyfsTer17
NM_001293190.1:c.667dup NP_001280119.1:p.Asp223GlyfsTer17
NM_001293191.1:c.655dup NP_001280120.1:p.Asp219GlyfsTer17
NM_001293192.1:c.346dup NP_001280121.1:p.Asp116GlyfsTer17
NM_001293195.1:c.622dup NP_001280124.1:p.Asp208GlyfsTer17
NM_001293196.1:c.346dup NP_001280125.1:p.Asp116GlyfsTer17
NM_012222.2:c.697dup NP_036354.1:p.Asp233GlyfsTer17
XM_011541497.1:c.682dup XP_011539799.1:p.Asp228GlyfsTer17
XM_011541498.1:c.664dup XP_011539800.1:p.Asp222GlyfsTer17
XM_011541499.1:c.664dup XP_011539801.1:p.Asp222GlyfsTer17
XM_011541500.1:c.664dup XP_011539802.1:p.Asp222GlyfsTer17
XM_011541501.1:c.664dup XP_011539803.1:p.Asp222GlyfsTer17
XM_011541502.1:c.664dup XP_011539804.1:p.Asp222GlyfsTer17
XM_011541503.1:c.664dup XP_011539805.1:p.Asp222GlyfsTer17
XM_011541504.1:c.655dup XP_011539806.1:p.Asp219GlyfsTer17
XM_011541505.1:c.244dup XP_011539807.1:p.Asp82GlyfsTer17
XM_011541506.1:c.244dup XP_011539808.1:p.Asp82GlyfsTer17
XM_011541507.1:c.235dup XP_011539809.1:p.Asp79GlyfsTer17
XM_011541508.1:c.250dup XP_011539810.1:p.Asp84GlyfsTer17
XR_946658.1:n.753dup
NM_001350650.1:c.277dup NP_001337579.1:p.Asp93GlyfsTer17
NM_001350651.1:c.277dup NP_001337580.1:p.Asp93GlyfsTer17
NR_146882.1:n.880dup
NR_146883.1:n.694dup
XM_011541497.3:c.682dup XP_011539799.1:p.Asp228GlyfsTer17
XM_011541500.3:c.664dup XP_011539802.1:p.Asp222GlyfsTer17
XM_011541501.2:c.664dup XP_011539803.1:p.Asp222GlyfsTer17
XM_011541502.2:c.664dup XP_011539804.1:p.Asp222GlyfsTer17
XM_011541503.2:c.664dup XP_011539805.1:p.Asp222GlyfsTer17
XM_011541504.2:c.655dup XP_011539806.1:p.Asp219GlyfsTer17
XM_011541505.2:c.244dup XP_011539807.1:p.Asp82GlyfsTer17
XM_011541506.2:c.244dup XP_011539808.1:p.Asp82GlyfsTer17
XM_017001331.1:c.664dup XP_016856820.1:p.Asp222GlyfsTer17
XM_017001332.1:c.664dup XP_016856821.1:p.Asp222GlyfsTer17
XM_017001333.1:c.664dup XP_016856822.1:p.Asp222GlyfsTer17
XM_017001334.1:c.625dup XP_016856823.1:p.Asp209GlyfsTer17
XM_017001335.1:c.346dup XP_016856824.1:p.Asp116GlyfsTer17
XM_017001336.1:c.277dup XP_016856825.1:p.Asp93GlyfsTer17
XM_017001337.1:c.277dup XP_016856826.1:p.Asp93GlyfsTer17
XM_024447244.1:c.277dup XP_024303012.1:p.Asp93GlyfsTer17
XM_024447245.1:c.277dup XP_024303013.1:p.Asp93GlyfsTer17
XM_024447248.1:c.235dup XP_024303016.1:p.Asp79GlyfsTer17
XM_024447249.1:c.106dup XP_024303017.1:p.Asp36GlyfsTer17
XM_024447250.1:c.106dup XP_024303018.1:p.Asp36GlyfsTer17
XM_024447251.1:c.106dup XP_024303019.1:p.Asp36GlyfsTer17
XR_001737190.1:n.667dup
XR_001737192.1:n.479dup
XR_002956643.1:n.659dup
XR_002956644.1:n.1194dup
XR_946658.2:n.767dup
NM_001048171.2:c.622dup NP_001041636.2:p.Asp208GlyfsTer17
NM_001128425.2:c.706dup MANE Plus Clinical NP_001121897.1:p.Asp236GlyfsTer17
NM_001048172.2:c.625dup NP_001041637.1:p.Asp209GlyfsTer17
NM_001048173.2:c.622dup NP_001041638.1:p.Asp208GlyfsTer17
NM_001048174.2:c.622dup MANE Select NP_001041639.1:p.Asp208GlyfsTer17
NM_001293190.2:c.667dup NP_001280119.1:p.Asp223GlyfsTer17
NM_001293191.2:c.655dup NP_001280120.1:p.Asp219GlyfsTer17
NM_001293192.2:c.346dup NP_001280121.1:p.Asp116GlyfsTer17
NM_001293195.2:c.622dup NP_001280124.1:p.Asp208GlyfsTer17
NM_001293196.2:c.346dup NP_001280125.1:p.Asp116GlyfsTer17
NM_001350650.2:c.277dup NP_001337579.1:p.Asp93GlyfsTer17
NM_001350651.2:c.277dup NP_001337580.1:p.Asp93GlyfsTer17
NM_012222.3:c.697dup NP_036354.1:p.Asp233GlyfsTer17
NR_146882.2:n.850dup
NR_146883.2:n.699dup