Canonical Allele Identifier: CA346731152

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480856C>A , CM000664.2:g.47480856C>A	GRCh38
NC_000002.11:g.47707995C>A , CM000664.1:g.47707995C>A	GRCh37
NC_000002.10:g.47561499C>A	NCBI36
NG_007110.2:g.82733C>A , LRG_218:g.82733C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000251.3:c.2619C>A MANE Select	NP_000242.1:p.Cys873Ter
ENST00000233146.7:c.2619C>A MANE Select	ENSP00000233146.2:p.Cys873Ter
NM_000251.2:c.2619C>A , LRG_218t1:c.2619C>A	NP_000242.1:p.Cys873Ter
NM_001258281.1:c.2421C>A	NP_001245210.1:p.Cys807Ter
ENST00000233146.6:c.2619C>A	ENSP00000233146.2:p.Cys873Ter
ENST00000406134.5:c.2619C>A	ENSP00000384199.1:p.Cys873Ter
ENST00000461394.5:n.60C>A
ENST00000543555.5:c.2421C>A	ENSP00000442697.1:p.Cys807Ter
ENST00000543555.6:c.2421C>A	ENSP00000442697.1:p.Cys807Ter
ENST00000610696.4:c.*1015C>A	ENSP00000483159.1:n.*1015C>A
ENST00000613514.4:c.*1159C>A	ENSP00000484137.1:n.*1159C>A
ENST00000617333.3:c.*1385C>A	ENSP00000482468.1:n.*1385C>A
ENST00000617938.4:c.*1591C>A	ENSP00000481158.1:n.*1591C>A
ENST00000621359.2:c.*185C>A	ENSP00000481416.1:n.*185C>A
ENST00000644092.1:c.*919C>A	ENSP00000496351.1:n.*919C>A
ENST00000644900.1:c.472C>A
ENST00000644900.2:c.2619C>A	ENSP00000495641.2:p.Cys873Ter
ENST00000645339.1:c.2619C>A	ENSP00000496441.1:p.Cys873Ter
ENST00000645506.1:c.2619C>A	ENSP00000495455.1:p.Cys873Ter
ENST00000646415.1:c.2619C>A	ENSP00000495543.1:p.Cys873Ter
XM_005264332.2:c.2619C>A	XP_005264389.2:p.Cys873Ter
XM_005264332.4:c.2619C>A	XP_005264389.2:p.Cys873Ter
XM_011532867.1:c.2619C>A	XP_011531169.1:p.Cys873Ter
XM_011532867.2:c.2619C>A	XP_011531169.1:p.Cys873Ter
XR_001738747.2:n.2681C>A
XR_939685.1:n.2691C>A
XR_939685.2:n.2681C>A