Canonical Allele Identifier: CA2495876101

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480800C= , CM000664.2:g.47480800C=	GRCh38
NC_000002.11:g.47707939C= , CM000664.1:g.47707939C=	GRCh37
NC_000002.10:g.47561443C=	NCBI36
NG_007110.2:g.82677C= , LRG_218:g.82677C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2563C=	ENSP00000495641.2:p.Gln855=
ENST00000233146.7:c.2563C= MANE Select	ENSP00000233146.2:p.Gln855=
ENST00000543555.6:c.2365C=	ENSP00000442697.1:p.Gln789=
ENST00000644092.1:c.*863C=	ENSP00000496351.1:n.*863C=
ENST00000644900.1:c.416C=
ENST00000645339.1:c.2563C=	ENSP00000496441.1:p.Gln855=
ENST00000645506.1:c.2563C=	ENSP00000495455.1:p.Gln855=
ENST00000646415.1:c.2563C=	ENSP00000495543.1:p.Gln855=
ENST00000233146.6:c.2563C=	ENSP00000233146.2:p.Gln855=
ENST00000406134.5:c.2563C=	ENSP00000384199.1:p.Gln855=
ENST00000461394.5:n.4C=
ENST00000543555.5:c.2365C=	ENSP00000442697.1:p.Gln789=
ENST00000610696.4:c.*959C=	ENSP00000483159.1:n.*959C=
ENST00000613514.4:c.*1103C=	ENSP00000484137.1:n.*1103C=
ENST00000617333.3:c.*1329C=	ENSP00000482468.1:n.*1329C=
ENST00000617938.4:c.*1535C=	ENSP00000481158.1:n.*1535C=
ENST00000621359.2:c.*129C=	ENSP00000481416.1:n.*129C=
NM_000251.2:c.2563C= , LRG_218t1:c.2563C=	NP_000242.1:p.Gln855=
NM_001258281.1:c.2365C=	NP_001245210.1:p.Gln789=
XM_005264332.2:c.2563C=	XP_005264389.2:p.Gln855=
XM_011532867.1:c.2563C=	XP_011531169.1:p.Gln855=
XR_939685.1:n.2635C=
XM_005264332.4:c.2563C=	XP_005264389.2:p.Gln855=
XM_011532867.2:c.2563C=	XP_011531169.1:p.Gln855=
XR_001738747.2:n.2625C=
XR_939685.2:n.2625C=
NM_000251.3:c.2563C= MANE Select	NP_000242.1:p.Gln855=