Canonical Allele Identifier: CA2473712686
Gene: MUTYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332365G>A , CM000663.2:g.45332365G>A GRCh38
NC_000001.10:g.45798037G>A , CM000663.1:g.45798037G>A GRCh37
NC_000001.9:g.45570624G>A NCBI36
NG_008189.1:g.13106C>T , LRG_220:g.13106C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000672818.3:c.779+26C>T ENSP00000500891.1:n.779+26C>T
ENST00000450313.6:c.*33+26C>T ENSP00000408176.2:n.*33+26C>T
ENST00000456914.7:c.704+26C>T MANE Select ENSP00000407590.2:n.704+26C>T
ENST00000461495.6:c.*443+26C>T ENSP00000437166.1:n.*443+26C>T
ENST00000671898.1:c.1292+26C>T ENSP00000499896.1:n.1292+26C>T
ENST00000672011.1:c.*33+26C>T ENSP00000500418.1:n.*33+26C>T
ENST00000672314.1:c.704+26C>T ENSP00000500828.1:n.704+26C>T
ENST00000672593.1:c.*703C>T ENSP00000500455.1:n.*703C>T
ENST00000672764.1:c.*33+26C>T ENSP00000500886.1:n.*33+26C>T
ENST00000672818.2:c.779+26C>T ENSP00000500891.1:n.779+26C>T
ENST00000673134.1:c.*401+26C>T ENSP00000500526.1:n.*401+26C>T
ENST00000674679.1:n.732+26C>T ENSP00000501623.1:n.732+26C>T
ENST00000354383.10:c.707+26C>T ENSP00000346354.6:n.707+26C>T
ENST00000355498.6:c.704+26C>T ENSP00000347685.2:n.704+26C>T
ENST00000372098.7:c.779+26C>T ENSP00000361170.3:n.779+26C>T
ENST00000372104.5:c.704+26C>T ENSP00000361176.1:n.704+26C>T
ENST00000372110.7:c.749+26C>T ENSP00000361182.3:n.749+26C>T
ENST00000372115.7:c.746+26C>T ENSP00000361187.3:n.746+26C>T
ENST00000412971.5:c.320+26C>T ENSP00000410263.1:n.320+26C>T
ENST00000435155.1:c.737+26C>T ENSP00000403655.1:n.737+26C>T
ENST00000448481.5:c.737+26C>T ENSP00000409718.1:n.737+26C>T
ENST00000450313.5:c.788+26C>T ENSP00000408176.1:n.788+26C>T
ENST00000456914.6:c.704+26C>T ENSP00000407590.2:n.704+26C>T
ENST00000461495.5:c.*443+26C>T ENSP00000437166.1:n.*443+26C>T
ENST00000462388.5:n.395+26C>T
ENST00000466231.1:n.15C>T
ENST00000467459.5:n.98+26C>T ENSP00000435889.1:n.98+26C>T
ENST00000467940.5:c.*627+26C>T ENSP00000436478.1:n.*627+26C>T
ENST00000470256.5:c.*33+26C>T ENSP00000434985.1:n.*33+26C>T
ENST00000475516.5:c.*517+26C>T ENSP00000433843.1:n.*517+26C>T
ENST00000478796.5:n.691+26C>T
ENST00000481571.5:c.*517+26C>T ENSP00000436597.1:n.*517+26C>T
ENST00000488731.6:c.187+398C>T ENSP00000432330.1:n.187+398C>T
ENST00000528013.6:c.746+26C>T ENSP00000433130.2:n.746+26C>T
ENST00000529984.5:c.187+398C>T ENSP00000437093.1:n.187+398C>T
ENST00000531105.5:c.115+2026C>T ENSP00000431292.1:n.115+2026C>T
ENST00000533178.5:n.333+26C>T ENSP00000436430.1:n.333+26C>T
NM_001048171.1:c.746+26C>T NP_001041636.1:n.746+26C>T
NM_001048172.1:c.707+26C>T NP_001041637.1:n.707+26C>T
NM_001048173.1:c.704+26C>T NP_001041638.1:n.704+26C>T
NM_001048174.1:c.704+26C>T NP_001041639.1:n.704+26C>T
NM_001128425.1:c.788+26C>T , LRG_220t1:c.788+26C>T NP_001121897.1:n.788+26C>T
NM_001293190.1:c.749+26C>T NP_001280119.1:n.749+26C>T
NM_001293191.1:c.737+26C>T NP_001280120.1:n.737+26C>T
NM_001293192.1:c.428+26C>T NP_001280121.1:n.428+26C>T
NM_001293195.1:c.704+26C>T NP_001280124.1:n.704+26C>T
NM_001293196.1:c.428+26C>T NP_001280125.1:n.428+26C>T
NM_012222.2:c.779+26C>T NP_036354.1:n.779+26C>T
XM_011541497.1:c.764+26C>T XP_011539799.1:n.764+26C>T
XM_011541498.1:c.746+26C>T XP_011539800.1:n.746+26C>T
XM_011541499.1:c.746+26C>T XP_011539801.1:n.746+26C>T
XM_011541500.1:c.746+26C>T XP_011539802.1:n.746+26C>T
XM_011541501.1:c.746+26C>T XP_011539803.1:n.746+26C>T
XM_011541502.1:c.746+26C>T XP_011539804.1:n.746+26C>T
XM_011541503.1:c.746+26C>T XP_011539805.1:n.746+26C>T
XM_011541504.1:c.737+26C>T XP_011539806.1:n.737+26C>T
XM_011541505.1:c.326+26C>T XP_011539807.1:n.326+26C>T
XM_011541506.1:c.326+26C>T XP_011539808.1:n.326+26C>T
XM_011541507.1:c.317+26C>T XP_011539809.1:n.317+26C>T
XM_011541508.1:c.332+26C>T XP_011539810.1:n.332+26C>T
XR_946658.1:n.835+26C>T
NM_001350650.1:c.359+26C>T NP_001337579.1:n.359+26C>T
NM_001350651.1:c.359+26C>T NP_001337580.1:n.359+26C>T
NR_146882.1:n.962+26C>T
NR_146883.1:n.776+26C>T
XM_011541497.3:c.764+26C>T XP_011539799.1:n.764+26C>T
XM_011541500.3:c.746+26C>T XP_011539802.1:n.746+26C>T
XM_011541501.2:c.746+26C>T XP_011539803.1:n.746+26C>T
XM_011541502.2:c.746+26C>T XP_011539804.1:n.746+26C>T
XM_011541503.2:c.746+26C>T XP_011539805.1:n.746+26C>T
XM_011541504.2:c.737+26C>T XP_011539806.1:n.737+26C>T
XM_011541505.2:c.326+26C>T XP_011539807.1:n.326+26C>T
XM_011541506.2:c.326+26C>T XP_011539808.1:n.326+26C>T
XM_017001331.1:c.746+26C>T XP_016856820.1:n.746+26C>T
XM_017001332.1:c.746+26C>T XP_016856821.1:n.746+26C>T
XM_017001333.1:c.746+26C>T XP_016856822.1:n.746+26C>T
XM_017001334.1:c.707+26C>T XP_016856823.1:n.707+26C>T
XM_017001335.1:c.428+26C>T XP_016856824.1:n.428+26C>T
XM_017001336.1:c.359+26C>T XP_016856825.1:n.359+26C>T
XM_017001337.1:c.359+26C>T XP_016856826.1:n.359+26C>T
XM_024447244.1:c.359+26C>T XP_024303012.1:n.359+26C>T
XM_024447245.1:c.359+26C>T XP_024303013.1:n.359+26C>T
XM_024447248.1:c.317+26C>T XP_024303016.1:n.317+26C>T
XM_024447249.1:c.188+26C>T XP_024303017.1:n.188+26C>T
XM_024447250.1:c.188+26C>T XP_024303018.1:n.188+26C>T
XM_024447251.1:c.188+26C>T XP_024303019.1:n.188+26C>T
XR_001737190.1:n.749+26C>T
XR_001737192.1:n.561+26C>T
XR_002956643.1:n.741+26C>T
XR_002956644.1:n.1276+26C>T
XR_946658.2:n.849+26C>T
NM_001048171.2:c.704+26C>T NP_001041636.2:n.704+26C>T
NM_001128425.2:c.788+26C>T NP_001121897.1:n.788+26C>T
NM_001048172.2:c.707+26C>T NP_001041637.1:n.707+26C>T
NM_001048173.2:c.704+26C>T NP_001041638.1:n.704+26C>T
NM_001048174.2:c.704+26C>T MANE Select NP_001041639.1:n.704+26C>T
NM_001293190.2:c.749+26C>T NP_001280119.1:n.749+26C>T
NM_001293191.2:c.737+26C>T NP_001280120.1:n.737+26C>T
NM_001293192.2:c.428+26C>T NP_001280121.1:n.428+26C>T
NM_001293195.2:c.704+26C>T NP_001280124.1:n.704+26C>T
NM_001293196.2:c.428+26C>T NP_001280125.1:n.428+26C>T
NM_001350650.2:c.359+26C>T NP_001337579.1:n.359+26C>T
NM_001350651.2:c.359+26C>T NP_001337580.1:n.359+26C>T
NM_012222.3:c.779+26C>T NP_036354.1:n.779+26C>T
NR_146882.2:n.932+26C>T
NR_146883.2:n.781+26C>T