Canonical Allele Identifier: CA340134890
Gene: MUTYH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332467T>A , CM000663.2:g.45332467T>A GRCh38
NC_000001.10:g.45798139T>A , CM000663.1:g.45798139T>A GRCh37
NC_000001.9:g.45570726T>A NCBI36
NG_008189.1:g.13004A>T , LRG_220:g.13004A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.244A>T ENSP00000410263.2:p.Asn82Tyr
ENST00000435155.2:c.661A>T ENSP00000403655.2:p.Asn221Tyr
ENST00000467459.6:c.628A>T ENSP00000435889.2:p.Asn210Tyr
ENST00000483127.2:c.646A>T ENSP00000436469.2:p.Asn216Tyr
ENST00000485271.6:c.628A>T ENSP00000431264.2:p.Asn210Tyr
ENST00000529892.6:c.670A>T ENSP00000432528.2:p.Asn224Tyr
ENST00000533178.6:c.251A>T ENSP00000436430.2:p.Gln84Leu
ENST00000672314.2:c.628A>T ENSP00000500828.2:p.Asn210Tyr
ENST00000674679.2:c.*540A>T ENSP00000501623.2:n.*540A>T
ENST00000710952.2:c.712A>T MANE Plus Clinical ENSP00000518552.2:p.Asn238Tyr
ENST00000672818.3:c.703A>T ENSP00000500891.1:p.Asn235Tyr
ENST00000450313.6:c.638A>T ENSP00000408176.2:p.Gln213Leu
ENST00000456914.7:c.628A>T MANE Select ENSP00000407590.2:p.Asn210Tyr
ENST00000461495.6:c.*367A>T ENSP00000437166.1:n.*367A>T
ENST00000671898.1:c.1216A>T ENSP00000499896.1:p.Asn406Tyr
ENST00000672011.1:c.596A>T ENSP00000500418.1:p.Gln199Leu
ENST00000672314.1:c.628A>T ENSP00000500828.1:p.Asn210Tyr
ENST00000672593.1:c.*601A>T ENSP00000500455.1:n.*601A>T
ENST00000672764.1:c.587A>T ENSP00000500886.1:p.Gln196Leu
ENST00000672818.2:c.703A>T ENSP00000500891.1:p.Asn235Tyr
ENST00000673134.1:c.*325A>T ENSP00000500526.1:n.*325A>T
ENST00000674679.1:c.656A>T ENSP00000501623.1:n.656A>T
ENST00000354383.10:c.631A>T ENSP00000346354.6:p.Asn211Tyr
ENST00000355498.6:c.628A>T ENSP00000347685.2:p.Asn210Tyr
ENST00000372098.7:c.703A>T ENSP00000361170.3:p.Asn235Tyr
ENST00000372104.5:c.628A>T ENSP00000361176.1:p.Asn210Tyr
ENST00000372110.7:c.673A>T ENSP00000361182.3:p.Asn225Tyr
ENST00000372115.7:c.670A>T ENSP00000361187.3:p.Asn224Tyr
ENST00000412971.5:c.244A>T ENSP00000410263.1:p.Asn82Tyr
ENST00000435155.1:c.661A>T ENSP00000403655.1:p.Asn221Tyr
ENST00000448481.5:c.661A>T ENSP00000409718.1:p.Asn221Tyr
ENST00000450313.5:c.712A>T ENSP00000408176.1:p.Asn238Tyr
ENST00000456914.6:c.628A>T ENSP00000407590.2:p.Asn210Tyr
ENST00000461495.5:c.*367A>T ENSP00000437166.1:n.*367A>T
ENST00000462388.5:n.319A>T
ENST00000467459.5:c.22A>T ENSP00000435889.1:p.Asn8Tyr
ENST00000467940.5:c.*551A>T ENSP00000436478.1:n.*551A>T
ENST00000470256.5:c.515A>T ENSP00000434985.1:p.Gln172Leu
ENST00000475516.5:c.*441A>T ENSP00000433843.1:n.*441A>T
ENST00000478796.5:n.615A>T
ENST00000481571.5:c.*441A>T ENSP00000436597.1:n.*441A>T
ENST00000488731.6:c.187+296A>T ENSP00000432330.1:n.187+296A>T
ENST00000525160.5:c.*279A>T ENSP00000431568.1:n.*279A>T
ENST00000528013.6:c.670A>T ENSP00000433130.2:p.Asn224Tyr
ENST00000529984.5:c.187+296A>T ENSP00000437093.1:n.187+296A>T
ENST00000531105.5:c.115+1924A>T ENSP00000431292.1:n.115+1924A>T
ENST00000533178.5:c.257A>T ENSP00000436430.1:p.Gln86Leu
NM_001048171.1:c.670A>T NP_001041636.1:p.Asn224Tyr
NM_001048172.1:c.631A>T NP_001041637.1:p.Asn211Tyr
NM_001048173.1:c.628A>T NP_001041638.1:p.Asn210Tyr
NM_001048174.1:c.628A>T NP_001041639.1:p.Asn210Tyr
NM_001128425.1:c.712A>T , LRG_220t1:c.712A>T NP_001121897.1:p.Asn238Tyr
NM_001293190.1:c.673A>T NP_001280119.1:p.Asn225Tyr
NM_001293191.1:c.661A>T NP_001280120.1:p.Asn221Tyr
NM_001293192.1:c.352A>T NP_001280121.1:p.Asn118Tyr
NM_001293195.1:c.628A>T NP_001280124.1:p.Asn210Tyr
NM_001293196.1:c.352A>T NP_001280125.1:p.Asn118Tyr
NM_012222.2:c.703A>T NP_036354.1:p.Asn235Tyr
XM_011541497.1:c.688A>T XP_011539799.1:p.Asn230Tyr
XM_011541498.1:c.670A>T XP_011539800.1:p.Asn224Tyr
XM_011541499.1:c.670A>T XP_011539801.1:p.Asn224Tyr
XM_011541500.1:c.670A>T XP_011539802.1:p.Asn224Tyr
XM_011541501.1:c.670A>T XP_011539803.1:p.Asn224Tyr
XM_011541502.1:c.670A>T XP_011539804.1:p.Asn224Tyr
XM_011541503.1:c.670A>T XP_011539805.1:p.Asn224Tyr
XM_011541504.1:c.661A>T XP_011539806.1:p.Asn221Tyr
XM_011541505.1:c.250A>T XP_011539807.1:p.Asn84Tyr
XM_011541506.1:c.250A>T XP_011539808.1:p.Asn84Tyr
XM_011541507.1:c.241A>T XP_011539809.1:p.Asn81Tyr
XM_011541508.1:c.256A>T XP_011539810.1:p.Asn86Tyr
XR_946658.1:n.759A>T
NM_001350650.1:c.283A>T NP_001337579.1:p.Asn95Tyr
NM_001350651.1:c.283A>T NP_001337580.1:p.Asn95Tyr
NR_146882.1:n.886A>T
NR_146883.1:n.700A>T
XM_011541497.3:c.688A>T XP_011539799.1:p.Asn230Tyr
XM_011541500.3:c.670A>T XP_011539802.1:p.Asn224Tyr
XM_011541501.2:c.670A>T XP_011539803.1:p.Asn224Tyr
XM_011541502.2:c.670A>T XP_011539804.1:p.Asn224Tyr
XM_011541503.2:c.670A>T XP_011539805.1:p.Asn224Tyr
XM_011541504.2:c.661A>T XP_011539806.1:p.Asn221Tyr
XM_011541505.2:c.250A>T XP_011539807.1:p.Asn84Tyr
XM_011541506.2:c.250A>T XP_011539808.1:p.Asn84Tyr
XM_017001331.1:c.670A>T XP_016856820.1:p.Asn224Tyr
XM_017001332.1:c.670A>T XP_016856821.1:p.Asn224Tyr
XM_017001333.1:c.670A>T XP_016856822.1:p.Asn224Tyr
XM_017001334.1:c.631A>T XP_016856823.1:p.Asn211Tyr
XM_017001335.1:c.352A>T XP_016856824.1:p.Asn118Tyr
XM_017001336.1:c.283A>T XP_016856825.1:p.Asn95Tyr
XM_017001337.1:c.283A>T XP_016856826.1:p.Asn95Tyr
XM_024447244.1:c.283A>T XP_024303012.1:p.Asn95Tyr
XM_024447245.1:c.283A>T XP_024303013.1:p.Asn95Tyr
XM_024447248.1:c.241A>T XP_024303016.1:p.Asn81Tyr
XM_024447249.1:c.112A>T XP_024303017.1:p.Asn38Tyr
XM_024447250.1:c.112A>T XP_024303018.1:p.Asn38Tyr
XM_024447251.1:c.112A>T XP_024303019.1:p.Asn38Tyr
XR_001737190.1:n.673A>T
XR_001737192.1:n.485A>T
XR_002956643.1:n.665A>T
XR_002956644.1:n.1200A>T
XR_946658.2:n.773A>T
NM_001048171.2:c.628A>T NP_001041636.2:p.Asn210Tyr
NM_001128425.2:c.712A>T MANE Plus Clinical NP_001121897.1:p.Asn238Tyr
NM_001048172.2:c.631A>T NP_001041637.1:p.Asn211Tyr
NM_001048173.2:c.628A>T NP_001041638.1:p.Asn210Tyr
NM_001048174.2:c.628A>T MANE Select NP_001041639.1:p.Asn210Tyr
NM_001293190.2:c.673A>T NP_001280119.1:p.Asn225Tyr
NM_001293191.2:c.661A>T NP_001280120.1:p.Asn221Tyr
NM_001293192.2:c.352A>T NP_001280121.1:p.Asn118Tyr
NM_001293195.2:c.628A>T NP_001280124.1:p.Asn210Tyr
NM_001293196.2:c.352A>T NP_001280125.1:p.Asn118Tyr
NM_001350650.2:c.283A>T NP_001337579.1:p.Asn95Tyr
NM_001350651.2:c.283A>T NP_001337580.1:p.Asn95Tyr
NM_012222.3:c.703A>T NP_036354.1:p.Asn235Tyr
NR_146882.2:n.856A>T
NR_146883.2:n.705A>T