Canonical Allele Identifier: CA340133872

Gene: MUTYH

Linked Data

• gnomAD v4: 1-45331829-G-T
• MyVariant Identifiers: chr1:g.45797501G>T (hg19) ; chr1:g.45331829G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45331829G>T , CM000663.2:g.45331829G>T	GRCh38
NC_000001.10:g.45797501G>T , CM000663.1:g.45797501G>T	GRCh37
NC_000001.9:g.45570088G>T	NCBI36
NG_008189.1:g.13642C>A , LRG_220:g.13642C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.550C>A	ENSP00000410263.2:p.His184Asn
ENST00000435155.2:c.967C>A	ENSP00000403655.2:p.His323Asn
ENST00000467459.6:c.957C>A	ENSP00000435889.2:p.Ala319=
ENST00000483127.2:c.952C>A	ENSP00000436469.2:p.His318Asn
ENST00000485271.6:c.934C>A	ENSP00000431264.2:p.His312Asn
ENST00000529892.6:c.955+194C>A	ENSP00000432528.2:n.955+194C>A
ENST00000533178.6:c.*263C>A	ENSP00000436430.2:n.*263C>A
ENST00000672314.2:c.934C>A	ENSP00000500828.2:p.His312Asn
ENST00000710952.2:c.1018C>A MANE Plus Clinical	ENSP00000518552.2:p.His340Asn
ENST00000672818.3:c.1009C>A	ENSP00000500891.1:p.His337Asn
ENST00000456914.7:c.934C>A MANE Select	ENSP00000407590.2:p.His312Asn
ENST00000671898.1:c.1522C>A	ENSP00000499896.1:p.His508Asn
ENST00000672011.1:c.*263C>A	ENSP00000500418.1:n.*263C>A
ENST00000672314.1:c.934C>A	ENSP00000500828.1:p.His312Asn
ENST00000672593.1:c.*1160C>A	ENSP00000500455.1:n.*1160C>A
ENST00000672764.1:c.*263C>A	ENSP00000500886.1:n.*263C>A
ENST00000672818.2:c.1009C>A	ENSP00000500891.1:p.His337Asn
ENST00000673134.1:c.*631C>A	ENSP00000500526.1:n.*631C>A
ENST00000354383.10:c.937C>A	ENSP00000346354.6:p.His313Asn
ENST00000355498.6:c.934C>A	ENSP00000347685.2:p.His312Asn
ENST00000372098.7:c.1009C>A	ENSP00000361170.3:p.His337Asn
ENST00000372104.5:c.934C>A	ENSP00000361176.1:p.His312Asn
ENST00000372110.7:c.979C>A	ENSP00000361182.3:p.His327Asn
ENST00000372115.7:c.976C>A	ENSP00000361187.3:p.His326Asn
ENST00000412971.5:c.550C>A	ENSP00000410263.1:p.His184Asn
ENST00000448481.5:c.967C>A	ENSP00000409718.1:p.His323Asn
ENST00000450313.5:c.1018C>A	ENSP00000408176.1:p.His340Asn
ENST00000456914.6:c.934C>A	ENSP00000407590.2:p.His312Asn
ENST00000462388.5:n.798C>A
ENST00000466231.1:n.299C>A
ENST00000467459.5:c.351C>A	ENSP00000435889.1:p.Ala117=
ENST00000475516.5:c.*747C>A	ENSP00000433843.1:n.*747C>A
ENST00000481571.5:c.*747C>A	ENSP00000436597.1:n.*747C>A
ENST00000482094.5:n.255C>A
ENST00000488731.6:c.188-273C>A	ENSP00000432330.1:n.188-273C>A
ENST00000528013.6:c.976C>A	ENSP00000433130.2:p.His326Asn
ENST00000529892.5:c.177+194C>A
ENST00000529984.5:c.188-273C>A	ENSP00000437093.1:n.188-273C>A
ENST00000531105.5:c.116-2392C>A	ENSP00000431292.1:n.116-2392C>A
ENST00000533178.5:c.563C>A	ENSP00000436430.1:n.563C>A
NM_001048171.1:c.976C>A	NP_001041636.1:p.His326Asn
NM_001048172.1:c.937C>A	NP_001041637.1:p.His313Asn
NM_001048173.1:c.934C>A	NP_001041638.1:p.His312Asn
NM_001048174.1:c.934C>A	NP_001041639.1:p.His312Asn
NM_001128425.1:c.1018C>A , LRG_220t1:c.1018C>A	NP_001121897.1:p.His340Asn
NM_001293190.1:c.979C>A	NP_001280119.1:p.His327Asn
NM_001293191.1:c.967C>A	NP_001280120.1:p.His323Asn
NM_001293192.1:c.658C>A	NP_001280121.1:p.His220Asn
NM_001293195.1:c.934C>A	NP_001280124.1:p.His312Asn
NM_001293196.1:c.658C>A	NP_001280125.1:p.His220Asn
NM_012222.2:c.1009C>A	NP_036354.1:p.His337Asn
XM_011541497.1:c.994C>A	XP_011539799.1:p.His332Asn
XM_011541498.1:c.976C>A	XP_011539800.1:p.His326Asn
XM_011541499.1:c.976C>A	XP_011539801.1:p.His326Asn
XM_011541500.1:c.976C>A	XP_011539802.1:p.His326Asn
XM_011541501.1:c.976C>A	XP_011539803.1:p.His326Asn
XM_011541502.1:c.976C>A	XP_011539804.1:p.His326Asn
XM_011541503.1:c.976C>A	XP_011539805.1:p.His326Asn
XM_011541504.1:c.967C>A	XP_011539806.1:p.His323Asn
XM_011541505.1:c.556C>A	XP_011539807.1:p.His186Asn
XM_011541506.1:c.556C>A	XP_011539808.1:p.His186Asn
XM_011541507.1:c.547C>A	XP_011539809.1:p.His183Asn
XM_011541508.1:c.562C>A	XP_011539810.1:p.His188Asn
XR_946658.1:n.1065C>A
NM_001350650.1:c.589C>A	NP_001337579.1:p.His197Asn
NM_001350651.1:c.589C>A	NP_001337580.1:p.His197Asn
NR_146882.1:n.1192C>A
NR_146883.1:n.1006C>A
XM_011541497.3:c.994C>A	XP_011539799.1:p.His332Asn
XM_011541500.3:c.976C>A	XP_011539802.1:p.His326Asn
XM_011541501.2:c.976C>A	XP_011539803.1:p.His326Asn
XM_011541502.2:c.976C>A	XP_011539804.1:p.His326Asn
XM_011541503.2:c.976C>A	XP_011539805.1:p.His326Asn
XM_011541504.2:c.967C>A	XP_011539806.1:p.His323Asn
XM_011541505.2:c.556C>A	XP_011539807.1:p.His186Asn
XM_011541506.2:c.556C>A	XP_011539808.1:p.His186Asn
XM_017001331.1:c.976C>A	XP_016856820.1:p.His326Asn
XM_017001332.1:c.976C>A	XP_016856821.1:p.His326Asn
XM_017001333.1:c.976C>A	XP_016856822.1:p.His326Asn
XM_017001334.1:c.937C>A	XP_016856823.1:p.His313Asn
XM_017001335.1:c.658C>A	XP_016856824.1:p.His220Asn
XM_017001336.1:c.589C>A	XP_016856825.1:p.His197Asn
XM_017001337.1:c.589C>A	XP_016856826.1:p.His197Asn
XM_024447244.1:c.589C>A	XP_024303012.1:p.His197Asn
XM_024447245.1:c.589C>A	XP_024303013.1:p.His197Asn
XM_024447248.1:c.547C>A	XP_024303016.1:p.His183Asn
XM_024447249.1:c.418C>A	XP_024303017.1:p.His140Asn
XM_024447250.1:c.418C>A	XP_024303018.1:p.His140Asn
XM_024447251.1:c.418C>A	XP_024303019.1:p.His140Asn
XR_001737190.1:n.979C>A
XR_001737192.1:n.791C>A
XR_002956643.1:n.971C>A
XR_002956644.1:n.1506C>A
XR_946658.2:n.1079C>A
NM_001048171.2:c.934C>A	NP_001041636.2:p.His312Asn
NM_001128425.2:c.1018C>A MANE Plus Clinical	NP_001121897.1:p.His340Asn
NM_001048172.2:c.937C>A	NP_001041637.1:p.His313Asn
NM_001048173.2:c.934C>A	NP_001041638.1:p.His312Asn
NM_001048174.2:c.934C>A MANE Select	NP_001041639.1:p.His312Asn
NM_001293190.2:c.979C>A	NP_001280119.1:p.His327Asn
NM_001293191.2:c.967C>A	NP_001280120.1:p.His323Asn
NM_001293192.2:c.658C>A	NP_001280121.1:p.His220Asn
NM_001293195.2:c.934C>A	NP_001280124.1:p.His312Asn
NM_001293196.2:c.658C>A	NP_001280125.1:p.His220Asn
NM_001350650.2:c.589C>A	NP_001337579.1:p.His197Asn
NM_001350651.2:c.589C>A	NP_001337580.1:p.His197Asn
NM_012222.3:c.1009C>A	NP_036354.1:p.His337Asn
NR_146882.2:n.1162C>A
NR_146883.2:n.1011C>A