Canonical Allele Identifier: CA417880190
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1161569
ClinVar RCV Id: RCV001506123
dbSNP Id: rs753807655
MyVariant Identifiers: chr1:g.45797952G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332280G>A , CM000663.2:g.45332280G>A GRCh38
NC_000001.10:g.45797952G>A , CM000663.1:g.45797952G>A GRCh37
NC_000001.9:g.45570539G>A NCBI36
NG_008189.1:g.13191C>T , LRG_220:g.13191C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.351C>T ENSP00000410263.2:p.Ala117=
ENST00000435155.2:c.768C>T ENSP00000403655.2:p.Ala256=
ENST00000467459.6:c.735C>T ENSP00000435889.2:p.Ala245=
ENST00000483127.2:c.753C>T ENSP00000436469.2:p.Ala251=
ENST00000485271.6:c.735C>T ENSP00000431264.2:p.Ala245=
ENST00000529892.6:c.777C>T ENSP00000432528.2:p.Ala259=
ENST00000533178.6:c.*64C>T ENSP00000436430.2:n.*64C>T
ENST00000672314.2:c.735C>T ENSP00000500828.2:p.Ala245=
ENST00000674679.2:c.*647C>T ENSP00000501623.2:n.*647C>T
ENST00000710952.2:c.819C>T MANE Plus Clinical ENSP00000518552.2:p.Ala273=
ENST00000672818.3:c.810C>T ENSP00000500891.1:p.Ala270=
ENST00000450313.6:c.*64C>T ENSP00000408176.2:n.*64C>T
ENST00000456914.7:c.735C>T MANE Select ENSP00000407590.2:p.Ala245=
ENST00000461495.6:c.*474C>T ENSP00000437166.1:n.*474C>T
ENST00000671898.1:c.1323C>T ENSP00000499896.1:p.Ala441=
ENST00000672011.1:c.*64C>T ENSP00000500418.1:n.*64C>T
ENST00000672314.1:c.735C>T ENSP00000500828.1:p.Ala245=
ENST00000672593.1:c.*788C>T ENSP00000500455.1:n.*788C>T
ENST00000672764.1:c.*64C>T ENSP00000500886.1:n.*64C>T
ENST00000672818.2:c.810C>T ENSP00000500891.1:p.Ala270=
ENST00000673134.1:c.*432C>T ENSP00000500526.1:n.*432C>T
ENST00000674679.1:c.763C>T ENSP00000501623.1:n.763C>T
ENST00000354383.10:c.738C>T ENSP00000346354.6:p.Ala246=
ENST00000355498.6:c.735C>T ENSP00000347685.2:p.Ala245=
ENST00000372098.7:c.810C>T ENSP00000361170.3:p.Ala270=
ENST00000372104.5:c.735C>T ENSP00000361176.1:p.Ala245=
ENST00000372110.7:c.780C>T ENSP00000361182.3:p.Ala260=
ENST00000372115.7:c.777C>T ENSP00000361187.3:p.Ala259=
ENST00000412971.5:c.351C>T ENSP00000410263.1:p.Ala117=
ENST00000435155.1:c.768C>T ENSP00000403655.1:p.Ala256=
ENST00000448481.5:c.768C>T ENSP00000409718.1:p.Ala256=
ENST00000450313.5:c.819C>T ENSP00000408176.1:p.Ala273=
ENST00000456914.6:c.735C>T ENSP00000407590.2:p.Ala245=
ENST00000461495.5:c.*474C>T ENSP00000437166.1:n.*474C>T
ENST00000462388.5:n.426C>T
ENST00000466231.1:n.100C>T
ENST00000467459.5:c.129C>T ENSP00000435889.1:p.Ala43=
ENST00000467940.5:c.*658C>T ENSP00000436478.1:n.*658C>T
ENST00000470256.5:c.*64C>T ENSP00000434985.1:n.*64C>T
ENST00000475516.5:c.*548C>T ENSP00000433843.1:n.*548C>T
ENST00000478796.5:n.722C>T
ENST00000481571.5:c.*548C>T ENSP00000436597.1:n.*548C>T
ENST00000488731.6:c.187+483C>T ENSP00000432330.1:n.187+483C>T
ENST00000528013.6:c.777C>T ENSP00000433130.2:p.Ala259=
ENST00000529984.5:c.187+483C>T ENSP00000437093.1:n.187+483C>T
ENST00000531105.5:c.115+2111C>T ENSP00000431292.1:n.115+2111C>T
ENST00000533178.5:c.364C>T ENSP00000436430.1:n.364C>T
NM_001048171.1:c.777C>T NP_001041636.1:p.Ala259=
NM_001048172.1:c.738C>T NP_001041637.1:p.Ala246=
NM_001048173.1:c.735C>T NP_001041638.1:p.Ala245=
NM_001048174.1:c.735C>T NP_001041639.1:p.Ala245=
NM_001128425.1:c.819C>T , LRG_220t1:c.819C>T NP_001121897.1:p.Ala273=
NM_001293190.1:c.780C>T NP_001280119.1:p.Ala260=
NM_001293191.1:c.768C>T NP_001280120.1:p.Ala256=
NM_001293192.1:c.459C>T NP_001280121.1:p.Ala153=
NM_001293195.1:c.735C>T NP_001280124.1:p.Ala245=
NM_001293196.1:c.459C>T NP_001280125.1:p.Ala153=
NM_012222.2:c.810C>T NP_036354.1:p.Ala270=
XM_011541497.1:c.795C>T XP_011539799.1:p.Ala265=
XM_011541498.1:c.777C>T XP_011539800.1:p.Ala259=
XM_011541499.1:c.777C>T XP_011539801.1:p.Ala259=
XM_011541500.1:c.777C>T XP_011539802.1:p.Ala259=
XM_011541501.1:c.777C>T XP_011539803.1:p.Ala259=
XM_011541502.1:c.777C>T XP_011539804.1:p.Ala259=
XM_011541503.1:c.777C>T XP_011539805.1:p.Ala259=
XM_011541504.1:c.768C>T XP_011539806.1:p.Ala256=
XM_011541505.1:c.357C>T XP_011539807.1:p.Ala119=
XM_011541506.1:c.357C>T XP_011539808.1:p.Ala119=
XM_011541507.1:c.348C>T XP_011539809.1:p.Ala116=
XM_011541508.1:c.363C>T XP_011539810.1:p.Ala121=
XR_946658.1:n.866C>T
NM_001350650.1:c.390C>T NP_001337579.1:p.Ala130=
NM_001350651.1:c.390C>T NP_001337580.1:p.Ala130=
NR_146882.1:n.993C>T
NR_146883.1:n.807C>T
XM_011541497.3:c.795C>T XP_011539799.1:p.Ala265=
XM_011541500.3:c.777C>T XP_011539802.1:p.Ala259=
XM_011541501.2:c.777C>T XP_011539803.1:p.Ala259=
XM_011541502.2:c.777C>T XP_011539804.1:p.Ala259=
XM_011541503.2:c.777C>T XP_011539805.1:p.Ala259=
XM_011541504.2:c.768C>T XP_011539806.1:p.Ala256=
XM_011541505.2:c.357C>T XP_011539807.1:p.Ala119=
XM_011541506.2:c.357C>T XP_011539808.1:p.Ala119=
XM_017001331.1:c.777C>T XP_016856820.1:p.Ala259=
XM_017001332.1:c.777C>T XP_016856821.1:p.Ala259=
XM_017001333.1:c.777C>T XP_016856822.1:p.Ala259=
XM_017001334.1:c.738C>T XP_016856823.1:p.Ala246=
XM_017001335.1:c.459C>T XP_016856824.1:p.Ala153=
XM_017001336.1:c.390C>T XP_016856825.1:p.Ala130=
XM_017001337.1:c.390C>T XP_016856826.1:p.Ala130=
XM_024447244.1:c.390C>T XP_024303012.1:p.Ala130=
XM_024447245.1:c.390C>T XP_024303013.1:p.Ala130=
XM_024447248.1:c.348C>T XP_024303016.1:p.Ala116=
XM_024447249.1:c.219C>T XP_024303017.1:p.Ala73=
XM_024447250.1:c.219C>T XP_024303018.1:p.Ala73=
XM_024447251.1:c.219C>T XP_024303019.1:p.Ala73=
XR_001737190.1:n.780C>T
XR_001737192.1:n.592C>T
XR_002956643.1:n.772C>T
XR_002956644.1:n.1307C>T
XR_946658.2:n.880C>T
NM_001048171.2:c.735C>T NP_001041636.2:p.Ala245=
NM_001128425.2:c.819C>T MANE Plus Clinical NP_001121897.1:p.Ala273=
NM_001048172.2:c.738C>T NP_001041637.1:p.Ala246=
NM_001048173.2:c.735C>T NP_001041638.1:p.Ala245=
NM_001048174.2:c.735C>T MANE Select NP_001041639.1:p.Ala245=
NM_001293190.2:c.780C>T NP_001280119.1:p.Ala260=
NM_001293191.2:c.768C>T NP_001280120.1:p.Ala256=
NM_001293192.2:c.459C>T NP_001280121.1:p.Ala153=
NM_001293195.2:c.735C>T NP_001280124.1:p.Ala245=
NM_001293196.2:c.459C>T NP_001280125.1:p.Ala153=
NM_001350650.2:c.390C>T NP_001337579.1:p.Ala130=
NM_001350651.2:c.390C>T NP_001337580.1:p.Ala130=
NM_012222.3:c.810C>T NP_036354.1:p.Ala270=
NR_146882.2:n.963C>T
NR_146883.2:n.812C>T