Canonical Allele Identifier: CA340134703
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1761726
ClinVar RCV Id: RCV002412416

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332297G>T , CM000663.2:g.45332297G>T GRCh38
NC_000001.10:g.45797969G>T , CM000663.1:g.45797969G>T GRCh37
NC_000001.9:g.45570556G>T NCBI36
NG_008189.1:g.13174C>A , LRG_220:g.13174C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.334C>A ENSP00000410263.2:p.Gln112Lys
ENST00000435155.2:c.751C>A ENSP00000403655.2:p.Gln251Lys
ENST00000467459.6:c.718C>A ENSP00000435889.2:p.Gln240Lys
ENST00000483127.2:c.736C>A ENSP00000436469.2:p.Gln246Lys
ENST00000485271.6:c.718C>A ENSP00000431264.2:p.Gln240Lys
ENST00000529892.6:c.760C>A ENSP00000432528.2:p.Gln254Lys
ENST00000533178.6:c.*47C>A ENSP00000436430.2:n.*47C>A
ENST00000672314.2:c.718C>A ENSP00000500828.2:p.Gln240Lys
ENST00000674679.2:c.*630C>A ENSP00000501623.2:n.*630C>A
ENST00000710952.2:c.802C>A MANE Plus Clinical ENSP00000518552.2:p.Gln268Lys
ENST00000672818.3:c.793C>A ENSP00000500891.1:p.Gln265Lys
ENST00000450313.6:c.*47C>A ENSP00000408176.2:n.*47C>A
ENST00000456914.7:c.718C>A MANE Select ENSP00000407590.2:p.Gln240Lys
ENST00000461495.6:c.*457C>A ENSP00000437166.1:n.*457C>A
ENST00000671898.1:c.1306C>A ENSP00000499896.1:p.Gln436Lys
ENST00000672011.1:c.*47C>A ENSP00000500418.1:n.*47C>A
ENST00000672314.1:c.718C>A ENSP00000500828.1:p.Gln240Lys
ENST00000672593.1:c.*771C>A ENSP00000500455.1:n.*771C>A
ENST00000672764.1:c.*47C>A ENSP00000500886.1:n.*47C>A
ENST00000672818.2:c.793C>A ENSP00000500891.1:p.Gln265Lys
ENST00000673134.1:c.*415C>A ENSP00000500526.1:n.*415C>A
ENST00000674679.1:c.746C>A ENSP00000501623.1:n.746C>A
ENST00000354383.10:c.721C>A ENSP00000346354.6:p.Gln241Lys
ENST00000355498.6:c.718C>A ENSP00000347685.2:p.Gln240Lys
ENST00000372098.7:c.793C>A ENSP00000361170.3:p.Gln265Lys
ENST00000372104.5:c.718C>A ENSP00000361176.1:p.Gln240Lys
ENST00000372110.7:c.763C>A ENSP00000361182.3:p.Gln255Lys
ENST00000372115.7:c.760C>A ENSP00000361187.3:p.Gln254Lys
ENST00000412971.5:c.334C>A ENSP00000410263.1:p.Gln112Lys
ENST00000435155.1:c.751C>A ENSP00000403655.1:p.Gln251Lys
ENST00000448481.5:c.751C>A ENSP00000409718.1:p.Gln251Lys
ENST00000450313.5:c.802C>A ENSP00000408176.1:p.Gln268Lys
ENST00000456914.6:c.718C>A ENSP00000407590.2:p.Gln240Lys
ENST00000461495.5:c.*457C>A ENSP00000437166.1:n.*457C>A
ENST00000462388.5:n.409C>A
ENST00000466231.1:n.83C>A
ENST00000467459.5:c.112C>A ENSP00000435889.1:p.Gln38Lys
ENST00000467940.5:c.*641C>A ENSP00000436478.1:n.*641C>A
ENST00000470256.5:c.*47C>A ENSP00000434985.1:n.*47C>A
ENST00000475516.5:c.*531C>A ENSP00000433843.1:n.*531C>A
ENST00000478796.5:n.705C>A
ENST00000481571.5:c.*531C>A ENSP00000436597.1:n.*531C>A
ENST00000488731.6:c.187+466C>A ENSP00000432330.1:n.187+466C>A
ENST00000528013.6:c.760C>A ENSP00000433130.2:p.Gln254Lys
ENST00000529984.5:c.187+466C>A ENSP00000437093.1:n.187+466C>A
ENST00000531105.5:c.115+2094C>A ENSP00000431292.1:n.115+2094C>A
ENST00000533178.5:c.347C>A ENSP00000436430.1:n.347C>A
NM_001048171.1:c.760C>A NP_001041636.1:p.Gln254Lys
NM_001048172.1:c.721C>A NP_001041637.1:p.Gln241Lys
NM_001048173.1:c.718C>A NP_001041638.1:p.Gln240Lys
NM_001048174.1:c.718C>A NP_001041639.1:p.Gln240Lys
NM_001128425.1:c.802C>A , LRG_220t1:c.802C>A NP_001121897.1:p.Gln268Lys
NM_001293190.1:c.763C>A NP_001280119.1:p.Gln255Lys
NM_001293191.1:c.751C>A NP_001280120.1:p.Gln251Lys
NM_001293192.1:c.442C>A NP_001280121.1:p.Gln148Lys
NM_001293195.1:c.718C>A NP_001280124.1:p.Gln240Lys
NM_001293196.1:c.442C>A NP_001280125.1:p.Gln148Lys
NM_012222.2:c.793C>A NP_036354.1:p.Gln265Lys
XM_011541497.1:c.778C>A XP_011539799.1:p.Gln260Lys
XM_011541498.1:c.760C>A XP_011539800.1:p.Gln254Lys
XM_011541499.1:c.760C>A XP_011539801.1:p.Gln254Lys
XM_011541500.1:c.760C>A XP_011539802.1:p.Gln254Lys
XM_011541501.1:c.760C>A XP_011539803.1:p.Gln254Lys
XM_011541502.1:c.760C>A XP_011539804.1:p.Gln254Lys
XM_011541503.1:c.760C>A XP_011539805.1:p.Gln254Lys
XM_011541504.1:c.751C>A XP_011539806.1:p.Gln251Lys
XM_011541505.1:c.340C>A XP_011539807.1:p.Gln114Lys
XM_011541506.1:c.340C>A XP_011539808.1:p.Gln114Lys
XM_011541507.1:c.331C>A XP_011539809.1:p.Gln111Lys
XM_011541508.1:c.346C>A XP_011539810.1:p.Gln116Lys
XR_946658.1:n.849C>A
NM_001350650.1:c.373C>A NP_001337579.1:p.Gln125Lys
NM_001350651.1:c.373C>A NP_001337580.1:p.Gln125Lys
NR_146882.1:n.976C>A
NR_146883.1:n.790C>A
XM_011541497.3:c.778C>A XP_011539799.1:p.Gln260Lys
XM_011541500.3:c.760C>A XP_011539802.1:p.Gln254Lys
XM_011541501.2:c.760C>A XP_011539803.1:p.Gln254Lys
XM_011541502.2:c.760C>A XP_011539804.1:p.Gln254Lys
XM_011541503.2:c.760C>A XP_011539805.1:p.Gln254Lys
XM_011541504.2:c.751C>A XP_011539806.1:p.Gln251Lys
XM_011541505.2:c.340C>A XP_011539807.1:p.Gln114Lys
XM_011541506.2:c.340C>A XP_011539808.1:p.Gln114Lys
XM_017001331.1:c.760C>A XP_016856820.1:p.Gln254Lys
XM_017001332.1:c.760C>A XP_016856821.1:p.Gln254Lys
XM_017001333.1:c.760C>A XP_016856822.1:p.Gln254Lys
XM_017001334.1:c.721C>A XP_016856823.1:p.Gln241Lys
XM_017001335.1:c.442C>A XP_016856824.1:p.Gln148Lys
XM_017001336.1:c.373C>A XP_016856825.1:p.Gln125Lys
XM_017001337.1:c.373C>A XP_016856826.1:p.Gln125Lys
XM_024447244.1:c.373C>A XP_024303012.1:p.Gln125Lys
XM_024447245.1:c.373C>A XP_024303013.1:p.Gln125Lys
XM_024447248.1:c.331C>A XP_024303016.1:p.Gln111Lys
XM_024447249.1:c.202C>A XP_024303017.1:p.Gln68Lys
XM_024447250.1:c.202C>A XP_024303018.1:p.Gln68Lys
XM_024447251.1:c.202C>A XP_024303019.1:p.Gln68Lys
XR_001737190.1:n.763C>A
XR_001737192.1:n.575C>A
XR_002956643.1:n.755C>A
XR_002956644.1:n.1290C>A
XR_946658.2:n.863C>A
NM_001048171.2:c.718C>A NP_001041636.2:p.Gln240Lys
NM_001128425.2:c.802C>A MANE Plus Clinical NP_001121897.1:p.Gln268Lys
NM_001048172.2:c.721C>A NP_001041637.1:p.Gln241Lys
NM_001048173.2:c.718C>A NP_001041638.1:p.Gln240Lys
NM_001048174.2:c.718C>A MANE Select NP_001041639.1:p.Gln240Lys
NM_001293190.2:c.763C>A NP_001280119.1:p.Gln255Lys
NM_001293191.2:c.751C>A NP_001280120.1:p.Gln251Lys
NM_001293192.2:c.442C>A NP_001280121.1:p.Gln148Lys
NM_001293195.2:c.718C>A NP_001280124.1:p.Gln240Lys
NM_001293196.2:c.442C>A NP_001280125.1:p.Gln148Lys
NM_001350650.2:c.373C>A NP_001337579.1:p.Gln125Lys
NM_001350651.2:c.373C>A NP_001337580.1:p.Gln125Lys
NM_012222.3:c.793C>A NP_036354.1:p.Gln265Lys
NR_146882.2:n.946C>A
NR_146883.2:n.795C>A