Canonical Allele Identifier: CA340134910
Gene: MUTYH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332473C>A , CM000663.2:g.45332473C>A GRCh38
NC_000001.10:g.45798145C>A , CM000663.1:g.45798145C>A GRCh37
NC_000001.9:g.45570732C>A NCBI36
NG_008189.1:g.12998G>T , LRG_220:g.12998G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.238G>T ENSP00000410263.2:p.Asp80Tyr
ENST00000435155.2:c.655G>T ENSP00000403655.2:p.Asp219Tyr
ENST00000467459.6:c.622G>T ENSP00000435889.2:p.Asp208Tyr
ENST00000483127.2:c.640G>T ENSP00000436469.2:p.Asp214Tyr
ENST00000485271.6:c.622G>T ENSP00000431264.2:p.Asp208Tyr
ENST00000529892.6:c.664G>T ENSP00000432528.2:p.Asp222Tyr
ENST00000533178.6:c.245G>T ENSP00000436430.2:p.Gly82Val
ENST00000672314.2:c.622G>T ENSP00000500828.2:p.Asp208Tyr
ENST00000674679.2:c.*534G>T ENSP00000501623.2:n.*534G>T
ENST00000710952.2:c.706G>T MANE Plus Clinical ENSP00000518552.2:p.Asp236Tyr
ENST00000672818.3:c.697G>T ENSP00000500891.1:p.Asp233Tyr
ENST00000450313.6:c.632G>T ENSP00000408176.2:p.Gly211Val
ENST00000456914.7:c.622G>T MANE Select ENSP00000407590.2:p.Asp208Tyr
ENST00000461495.6:c.*361G>T ENSP00000437166.1:n.*361G>T
ENST00000671898.1:c.1210G>T ENSP00000499896.1:p.Asp404Tyr
ENST00000672011.1:c.590G>T ENSP00000500418.1:p.Gly197Val
ENST00000672314.1:c.622G>T ENSP00000500828.1:p.Asp208Tyr
ENST00000672593.1:c.*595G>T ENSP00000500455.1:n.*595G>T
ENST00000672764.1:c.581G>T ENSP00000500886.1:p.Gly194Val
ENST00000672818.2:c.697G>T ENSP00000500891.1:p.Asp233Tyr
ENST00000673134.1:c.*319G>T ENSP00000500526.1:n.*319G>T
ENST00000674679.1:c.650G>T ENSP00000501623.1:n.650G>T
ENST00000354383.10:c.625G>T ENSP00000346354.6:p.Asp209Tyr
ENST00000355498.6:c.622G>T ENSP00000347685.2:p.Asp208Tyr
ENST00000372098.7:c.697G>T ENSP00000361170.3:p.Asp233Tyr
ENST00000372104.5:c.622G>T ENSP00000361176.1:p.Asp208Tyr
ENST00000372110.7:c.667G>T ENSP00000361182.3:p.Asp223Tyr
ENST00000372115.7:c.664G>T ENSP00000361187.3:p.Asp222Tyr
ENST00000412971.5:c.238G>T ENSP00000410263.1:p.Asp80Tyr
ENST00000435155.1:c.655G>T ENSP00000403655.1:p.Asp219Tyr
ENST00000448481.5:c.655G>T ENSP00000409718.1:p.Asp219Tyr
ENST00000450313.5:c.706G>T ENSP00000408176.1:p.Asp236Tyr
ENST00000456914.6:c.622G>T ENSP00000407590.2:p.Asp208Tyr
ENST00000461495.5:c.*361G>T ENSP00000437166.1:n.*361G>T
ENST00000462388.5:n.313G>T
ENST00000467459.5:c.16G>T ENSP00000435889.1:p.Asp6Tyr
ENST00000467940.5:c.*545G>T ENSP00000436478.1:n.*545G>T
ENST00000470256.5:c.509G>T ENSP00000434985.1:p.Gly170Val
ENST00000475516.5:c.*435G>T ENSP00000433843.1:n.*435G>T
ENST00000478796.5:n.609G>T
ENST00000481571.5:c.*435G>T ENSP00000436597.1:n.*435G>T
ENST00000488731.6:c.187+290G>T ENSP00000432330.1:n.187+290G>T
ENST00000525160.5:c.*273G>T ENSP00000431568.1:n.*273G>T
ENST00000528013.6:c.664G>T ENSP00000433130.2:p.Asp222Tyr
ENST00000529984.5:c.187+290G>T ENSP00000437093.1:n.187+290G>T
ENST00000531105.5:c.115+1918G>T ENSP00000431292.1:n.115+1918G>T
ENST00000533178.5:c.251G>T ENSP00000436430.1:p.Gly84Val
NM_001048171.1:c.664G>T NP_001041636.1:p.Asp222Tyr
NM_001048172.1:c.625G>T NP_001041637.1:p.Asp209Tyr
NM_001048173.1:c.622G>T NP_001041638.1:p.Asp208Tyr
NM_001048174.1:c.622G>T NP_001041639.1:p.Asp208Tyr
NM_001128425.1:c.706G>T , LRG_220t1:c.706G>T NP_001121897.1:p.Asp236Tyr
NM_001293190.1:c.667G>T NP_001280119.1:p.Asp223Tyr
NM_001293191.1:c.655G>T NP_001280120.1:p.Asp219Tyr
NM_001293192.1:c.346G>T NP_001280121.1:p.Asp116Tyr
NM_001293195.1:c.622G>T NP_001280124.1:p.Asp208Tyr
NM_001293196.1:c.346G>T NP_001280125.1:p.Asp116Tyr
NM_012222.2:c.697G>T NP_036354.1:p.Asp233Tyr
XM_011541497.1:c.682G>T XP_011539799.1:p.Asp228Tyr
XM_011541498.1:c.664G>T XP_011539800.1:p.Asp222Tyr
XM_011541499.1:c.664G>T XP_011539801.1:p.Asp222Tyr
XM_011541500.1:c.664G>T XP_011539802.1:p.Asp222Tyr
XM_011541501.1:c.664G>T XP_011539803.1:p.Asp222Tyr
XM_011541502.1:c.664G>T XP_011539804.1:p.Asp222Tyr
XM_011541503.1:c.664G>T XP_011539805.1:p.Asp222Tyr
XM_011541504.1:c.655G>T XP_011539806.1:p.Asp219Tyr
XM_011541505.1:c.244G>T XP_011539807.1:p.Asp82Tyr
XM_011541506.1:c.244G>T XP_011539808.1:p.Asp82Tyr
XM_011541507.1:c.235G>T XP_011539809.1:p.Asp79Tyr
XM_011541508.1:c.250G>T XP_011539810.1:p.Asp84Tyr
XR_946658.1:n.753G>T
NM_001350650.1:c.277G>T NP_001337579.1:p.Asp93Tyr
NM_001350651.1:c.277G>T NP_001337580.1:p.Asp93Tyr
NR_146882.1:n.880G>T
NR_146883.1:n.694G>T
XM_011541497.3:c.682G>T XP_011539799.1:p.Asp228Tyr
XM_011541500.3:c.664G>T XP_011539802.1:p.Asp222Tyr
XM_011541501.2:c.664G>T XP_011539803.1:p.Asp222Tyr
XM_011541502.2:c.664G>T XP_011539804.1:p.Asp222Tyr
XM_011541503.2:c.664G>T XP_011539805.1:p.Asp222Tyr
XM_011541504.2:c.655G>T XP_011539806.1:p.Asp219Tyr
XM_011541505.2:c.244G>T XP_011539807.1:p.Asp82Tyr
XM_011541506.2:c.244G>T XP_011539808.1:p.Asp82Tyr
XM_017001331.1:c.664G>T XP_016856820.1:p.Asp222Tyr
XM_017001332.1:c.664G>T XP_016856821.1:p.Asp222Tyr
XM_017001333.1:c.664G>T XP_016856822.1:p.Asp222Tyr
XM_017001334.1:c.625G>T XP_016856823.1:p.Asp209Tyr
XM_017001335.1:c.346G>T XP_016856824.1:p.Asp116Tyr
XM_017001336.1:c.277G>T XP_016856825.1:p.Asp93Tyr
XM_017001337.1:c.277G>T XP_016856826.1:p.Asp93Tyr
XM_024447244.1:c.277G>T XP_024303012.1:p.Asp93Tyr
XM_024447245.1:c.277G>T XP_024303013.1:p.Asp93Tyr
XM_024447248.1:c.235G>T XP_024303016.1:p.Asp79Tyr
XM_024447249.1:c.106G>T XP_024303017.1:p.Asp36Tyr
XM_024447250.1:c.106G>T XP_024303018.1:p.Asp36Tyr
XM_024447251.1:c.106G>T XP_024303019.1:p.Asp36Tyr
XR_001737190.1:n.667G>T
XR_001737192.1:n.479G>T
XR_002956643.1:n.659G>T
XR_002956644.1:n.1194G>T
XR_946658.2:n.767G>T
NM_001048171.2:c.622G>T NP_001041636.2:p.Asp208Tyr
NM_001128425.2:c.706G>T MANE Plus Clinical NP_001121897.1:p.Asp236Tyr
NM_001048172.2:c.625G>T NP_001041637.1:p.Asp209Tyr
NM_001048173.2:c.622G>T NP_001041638.1:p.Asp208Tyr
NM_001048174.2:c.622G>T MANE Select NP_001041639.1:p.Asp208Tyr
NM_001293190.2:c.667G>T NP_001280119.1:p.Asp223Tyr
NM_001293191.2:c.655G>T NP_001280120.1:p.Asp219Tyr
NM_001293192.2:c.346G>T NP_001280121.1:p.Asp116Tyr
NM_001293195.2:c.622G>T NP_001280124.1:p.Asp208Tyr
NM_001293196.2:c.346G>T NP_001280125.1:p.Asp116Tyr
NM_001350650.2:c.277G>T NP_001337579.1:p.Asp93Tyr
NM_001350651.2:c.277G>T NP_001337580.1:p.Asp93Tyr
NM_012222.3:c.697G>T NP_036354.1:p.Asp233Tyr
NR_146882.2:n.850G>T
NR_146883.2:n.699G>T