Canonical Allele Identifier: CA2495874622

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47478455T= , CM000664.2:g.47478455T=	GRCh38
NC_000002.11:g.47705594T= , CM000664.1:g.47705594T=	GRCh37
NC_000002.10:g.47559098T=	NCBI36
NG_007110.2:g.80332T= , LRG_218:g.80332T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2394T=	ENSP00000495641.2:p.Asn798=
ENST00000233146.7:c.2394T= MANE Select	ENSP00000233146.2:p.Asn798=
ENST00000543555.6:c.2196T=	ENSP00000442697.1:p.Asn732=
ENST00000644092.1:c.*694T=	ENSP00000496351.1:n.*694T=
ENST00000644900.1:c.247T=
ENST00000645339.1:c.2394T=	ENSP00000496441.1:p.Asn798=
ENST00000645506.1:c.2394T=	ENSP00000495455.1:p.Asn798=
ENST00000646415.1:c.2394T=	ENSP00000495543.1:p.Asn798=
ENST00000233146.6:c.2394T=	ENSP00000233146.2:p.Asn798=
ENST00000406134.5:c.2394T=	ENSP00000384199.1:p.Asn798=
ENST00000543555.5:c.2196T=	ENSP00000442697.1:p.Asn732=
ENST00000610696.4:c.*790T=	ENSP00000483159.1:n.*790T=
ENST00000613514.4:c.*934T=	ENSP00000484137.1:n.*934T=
ENST00000617333.3:c.*1160T=	ENSP00000482468.1:n.*1160T=
ENST00000617938.4:c.*1366T=	ENSP00000481158.1:n.*1366T=
ENST00000621359.2:c.2393T=	ENSP00000481416.1:p.Ile798=
NM_000251.2:c.2394T= , LRG_218t1:c.2394T=	NP_000242.1:p.Asn798=
NM_001258281.1:c.2196T=	NP_001245210.1:p.Asn732=
XM_005264332.2:c.2394T=	XP_005264389.2:p.Asn798=
XM_011532867.1:c.2394T=	XP_011531169.1:p.Asn798=
XR_939685.1:n.2466T=
XM_005264332.4:c.2394T=	XP_005264389.2:p.Asn798=
XM_011532867.2:c.2394T=	XP_011531169.1:p.Asn798=
XR_001738747.2:n.2456T=
XR_939685.2:n.2456T=
NM_000251.3:c.2394T= MANE Select	NP_000242.1:p.Asn798=