Canonical Allele Identifier: CA21837263
Gene: MUTYH HGNC NCBI

Linked Data

dbSNP Id: rs538252377

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332364A>G , CM000663.2:g.45332364A>G GRCh38
NC_000001.10:g.45798036A>G , CM000663.1:g.45798036A>G GRCh37
NC_000001.9:g.45570623A>G NCBI36
NG_008189.1:g.13107T>C , LRG_220:g.13107T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000672818.3:c.779+27T>C ENSP00000500891.1:n.779+27T>C
ENST00000450313.6:c.*33+27T>C ENSP00000408176.2:n.*33+27T>C
ENST00000456914.7:c.704+27T>C MANE Select ENSP00000407590.2:n.704+27T>C
ENST00000461495.6:c.*443+27T>C ENSP00000437166.1:n.*443+27T>C
ENST00000671898.1:c.1292+27T>C ENSP00000499896.1:n.1292+27T>C
ENST00000672011.1:c.*33+27T>C ENSP00000500418.1:n.*33+27T>C
ENST00000672314.1:c.704+27T>C ENSP00000500828.1:n.704+27T>C
ENST00000672593.1:c.*704T>C ENSP00000500455.1:n.*704T>C
ENST00000672764.1:c.*33+27T>C ENSP00000500886.1:n.*33+27T>C
ENST00000672818.2:c.779+27T>C ENSP00000500891.1:n.779+27T>C
ENST00000673134.1:c.*401+27T>C ENSP00000500526.1:n.*401+27T>C
ENST00000674679.1:n.732+27T>C ENSP00000501623.1:n.732+27T>C
ENST00000354383.10:c.707+27T>C ENSP00000346354.6:n.707+27T>C
ENST00000355498.6:c.704+27T>C ENSP00000347685.2:n.704+27T>C
ENST00000372098.7:c.779+27T>C ENSP00000361170.3:n.779+27T>C
ENST00000372104.5:c.704+27T>C ENSP00000361176.1:n.704+27T>C
ENST00000372110.7:c.749+27T>C ENSP00000361182.3:n.749+27T>C
ENST00000372115.7:c.746+27T>C ENSP00000361187.3:n.746+27T>C
ENST00000412971.5:c.320+27T>C ENSP00000410263.1:n.320+27T>C
ENST00000435155.1:c.737+27T>C ENSP00000403655.1:n.737+27T>C
ENST00000448481.5:c.737+27T>C ENSP00000409718.1:n.737+27T>C
ENST00000450313.5:c.788+27T>C ENSP00000408176.1:n.788+27T>C
ENST00000456914.6:c.704+27T>C ENSP00000407590.2:n.704+27T>C
ENST00000461495.5:c.*443+27T>C ENSP00000437166.1:n.*443+27T>C
ENST00000462388.5:n.395+27T>C
ENST00000466231.1:n.16T>C
ENST00000467459.5:n.98+27T>C ENSP00000435889.1:n.98+27T>C
ENST00000467940.5:c.*627+27T>C ENSP00000436478.1:n.*627+27T>C
ENST00000470256.5:c.*33+27T>C ENSP00000434985.1:n.*33+27T>C
ENST00000475516.5:c.*517+27T>C ENSP00000433843.1:n.*517+27T>C
ENST00000478796.5:n.691+27T>C
ENST00000481571.5:c.*517+27T>C ENSP00000436597.1:n.*517+27T>C
ENST00000488731.6:c.187+399T>C ENSP00000432330.1:n.187+399T>C
ENST00000528013.6:c.746+27T>C ENSP00000433130.2:n.746+27T>C
ENST00000529984.5:c.187+399T>C ENSP00000437093.1:n.187+399T>C
ENST00000531105.5:c.115+2027T>C ENSP00000431292.1:n.115+2027T>C
ENST00000533178.5:n.333+27T>C ENSP00000436430.1:n.333+27T>C
NM_001048171.1:c.746+27T>C NP_001041636.1:n.746+27T>C
NM_001048172.1:c.707+27T>C NP_001041637.1:n.707+27T>C
NM_001048173.1:c.704+27T>C NP_001041638.1:n.704+27T>C
NM_001048174.1:c.704+27T>C NP_001041639.1:n.704+27T>C
NM_001128425.1:c.788+27T>C , LRG_220t1:c.788+27T>C NP_001121897.1:n.788+27T>C
NM_001293190.1:c.749+27T>C NP_001280119.1:n.749+27T>C
NM_001293191.1:c.737+27T>C NP_001280120.1:n.737+27T>C
NM_001293192.1:c.428+27T>C NP_001280121.1:n.428+27T>C
NM_001293195.1:c.704+27T>C NP_001280124.1:n.704+27T>C
NM_001293196.1:c.428+27T>C NP_001280125.1:n.428+27T>C
NM_012222.2:c.779+27T>C NP_036354.1:n.779+27T>C
XM_011541497.1:c.764+27T>C XP_011539799.1:n.764+27T>C
XM_011541498.1:c.746+27T>C XP_011539800.1:n.746+27T>C
XM_011541499.1:c.746+27T>C XP_011539801.1:n.746+27T>C
XM_011541500.1:c.746+27T>C XP_011539802.1:n.746+27T>C
XM_011541501.1:c.746+27T>C XP_011539803.1:n.746+27T>C
XM_011541502.1:c.746+27T>C XP_011539804.1:n.746+27T>C
XM_011541503.1:c.746+27T>C XP_011539805.1:n.746+27T>C
XM_011541504.1:c.737+27T>C XP_011539806.1:n.737+27T>C
XM_011541505.1:c.326+27T>C XP_011539807.1:n.326+27T>C
XM_011541506.1:c.326+27T>C XP_011539808.1:n.326+27T>C
XM_011541507.1:c.317+27T>C XP_011539809.1:n.317+27T>C
XM_011541508.1:c.332+27T>C XP_011539810.1:n.332+27T>C
XR_946658.1:n.835+27T>C
NM_001350650.1:c.359+27T>C NP_001337579.1:n.359+27T>C
NM_001350651.1:c.359+27T>C NP_001337580.1:n.359+27T>C
NR_146882.1:n.962+27T>C
NR_146883.1:n.776+27T>C
XM_011541497.3:c.764+27T>C XP_011539799.1:n.764+27T>C
XM_011541500.3:c.746+27T>C XP_011539802.1:n.746+27T>C
XM_011541501.2:c.746+27T>C XP_011539803.1:n.746+27T>C
XM_011541502.2:c.746+27T>C XP_011539804.1:n.746+27T>C
XM_011541503.2:c.746+27T>C XP_011539805.1:n.746+27T>C
XM_011541504.2:c.737+27T>C XP_011539806.1:n.737+27T>C
XM_011541505.2:c.326+27T>C XP_011539807.1:n.326+27T>C
XM_011541506.2:c.326+27T>C XP_011539808.1:n.326+27T>C
XM_017001331.1:c.746+27T>C XP_016856820.1:n.746+27T>C
XM_017001332.1:c.746+27T>C XP_016856821.1:n.746+27T>C
XM_017001333.1:c.746+27T>C XP_016856822.1:n.746+27T>C
XM_017001334.1:c.707+27T>C XP_016856823.1:n.707+27T>C
XM_017001335.1:c.428+27T>C XP_016856824.1:n.428+27T>C
XM_017001336.1:c.359+27T>C XP_016856825.1:n.359+27T>C
XM_017001337.1:c.359+27T>C XP_016856826.1:n.359+27T>C
XM_024447244.1:c.359+27T>C XP_024303012.1:n.359+27T>C
XM_024447245.1:c.359+27T>C XP_024303013.1:n.359+27T>C
XM_024447248.1:c.317+27T>C XP_024303016.1:n.317+27T>C
XM_024447249.1:c.188+27T>C XP_024303017.1:n.188+27T>C
XM_024447250.1:c.188+27T>C XP_024303018.1:n.188+27T>C
XM_024447251.1:c.188+27T>C XP_024303019.1:n.188+27T>C
XR_001737190.1:n.749+27T>C
XR_001737192.1:n.561+27T>C
XR_002956643.1:n.741+27T>C
XR_002956644.1:n.1276+27T>C
XR_946658.2:n.849+27T>C
NM_001048171.2:c.704+27T>C NP_001041636.2:n.704+27T>C
NM_001128425.2:c.788+27T>C NP_001121897.1:n.788+27T>C
NM_001048172.2:c.707+27T>C NP_001041637.1:n.707+27T>C
NM_001048173.2:c.704+27T>C NP_001041638.1:n.704+27T>C
NM_001048174.2:c.704+27T>C MANE Select NP_001041639.1:n.704+27T>C
NM_001293190.2:c.749+27T>C NP_001280119.1:n.749+27T>C
NM_001293191.2:c.737+27T>C NP_001280120.1:n.737+27T>C
NM_001293192.2:c.428+27T>C NP_001280121.1:n.428+27T>C
NM_001293195.2:c.704+27T>C NP_001280124.1:n.704+27T>C
NM_001293196.2:c.428+27T>C NP_001280125.1:n.428+27T>C
NM_001350650.2:c.359+27T>C NP_001337579.1:n.359+27T>C
NM_001350651.2:c.359+27T>C NP_001337580.1:n.359+27T>C
NM_012222.3:c.779+27T>C NP_036354.1:n.779+27T>C
NR_146882.2:n.932+27T>C
NR_146883.2:n.781+27T>C