Canonical Allele Identifier: CA2495874582

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47478408C= , CM000664.2:g.47478408C=	GRCh38
NC_000002.11:g.47705547C= , CM000664.1:g.47705547C=	GRCh37
NC_000002.10:g.47559051C=	NCBI36
NG_007110.2:g.80285C= , LRG_218:g.80285C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2347C=	ENSP00000495641.2:p.His783=
ENST00000233146.7:c.2347C= MANE Select	ENSP00000233146.2:p.His783=
ENST00000543555.6:c.2149C=	ENSP00000442697.1:p.His717=
ENST00000644092.1:c.*647C=	ENSP00000496351.1:n.*647C=
ENST00000644900.1:c.200C=
ENST00000645339.1:c.2347C=	ENSP00000496441.1:p.His783=
ENST00000645506.1:c.2347C=	ENSP00000495455.1:p.His783=
ENST00000646415.1:c.2347C=	ENSP00000495543.1:p.His783=
ENST00000233146.6:c.2347C=	ENSP00000233146.2:p.His783=
ENST00000406134.5:c.2347C=	ENSP00000384199.1:p.His783=
ENST00000543555.5:c.2149C=	ENSP00000442697.1:p.His717=
ENST00000610696.4:c.*743C=	ENSP00000483159.1:n.*743C=
ENST00000613514.4:c.*887C=	ENSP00000484137.1:n.*887C=
ENST00000617333.3:c.*1113C=	ENSP00000482468.1:n.*1113C=
ENST00000617938.4:c.*1319C=	ENSP00000481158.1:n.*1319C=
ENST00000621359.2:c.2347-1C=	ENSP00000481416.1:n.2347-1C=
NM_000251.2:c.2347C= , LRG_218t1:c.2347C=	NP_000242.1:p.His783=
NM_001258281.1:c.2149C=	NP_001245210.1:p.His717=
XM_005264332.2:c.2347C=	XP_005264389.2:p.His783=
XM_011532867.1:c.2347C=	XP_011531169.1:p.His783=
XR_939685.1:n.2419C=
XM_005264332.4:c.2347C=	XP_005264389.2:p.His783=
XM_011532867.2:c.2347C=	XP_011531169.1:p.His783=
XR_001738747.2:n.2409C=
XR_939685.2:n.2409C=
NM_000251.3:c.2347C= MANE Select	NP_000242.1:p.His783=