Canonical Allele Identifier: CA2495877368

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47482903A= , CM000664.2:g.47482903A=	GRCh38
NC_000002.11:g.47710042A= , CM000664.1:g.47710042A=	GRCh37
NC_000002.10:g.47563546A=	NCBI36
NG_007110.2:g.84780A= , LRG_218:g.84780A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+2032A=	ENSP00000495641.2:n.2634+2032A=
ENST00000233146.7:c.2759A= MANE Select	ENSP00000233146.2:p.Asn920=
ENST00000543555.6:c.2561A=	ENSP00000442697.1:p.Asn854=
ENST00000644092.1:c.*934+2032A=	ENSP00000496351.1:n.*934+2032A=
ENST00000644900.1:c.487+2032A=
ENST00000645339.1:c.2634+2032A=	ENSP00000496441.1:n.2634+2032A=
ENST00000645506.1:c.2634+2032A=	ENSP00000495455.1:n.2634+2032A=
ENST00000646415.1:c.2634+2032A=	ENSP00000495543.1:n.2634+2032A=
ENST00000233146.6:c.2759A=	ENSP00000233146.2:p.Asn920=
ENST00000406134.5:c.2634+2032A=	ENSP00000384199.1:n.2634+2032A=
ENST00000461394.5:n.75+2032A=
ENST00000543555.5:c.2561A=	ENSP00000442697.1:p.Asn854=
ENST00000610696.4:c.*1155A=	ENSP00000483159.1:n.*1155A=
ENST00000613514.4:c.*1299A=	ENSP00000484137.1:n.*1299A=
ENST00000617333.3:c.*1525A=	ENSP00000482468.1:n.*1525A=
ENST00000617938.4:c.*1731A=	ENSP00000481158.1:n.*1731A=
ENST00000621359.2:c.*325A=	ENSP00000481416.1:n.*325A=
NM_000251.2:c.2759A= , LRG_218t1:c.2759A=	NP_000242.1:p.Asn920=
NM_001258281.1:c.2561A=	NP_001245210.1:p.Asn854=
XM_005264332.2:c.2634+2032A=	XP_005264389.2:n.2634+2032A=
XM_011532867.1:c.2634+2032A=	XP_011531169.1:n.2634+2032A=
XR_939685.1:n.2706+2032A=
XM_005264332.4:c.2634+2032A=	XP_005264389.2:n.2634+2032A=
XM_011532867.2:c.2634+2032A=	XP_011531169.1:n.2634+2032A=
XR_001738747.2:n.2696+2032A=
XR_939685.2:n.2696+2032A=
NM_000251.3:c.2759A= MANE Select	NP_000242.1:p.Asn920=