Canonical Allele Identifier: CA346730091

Gene: MSH2

Linked Data

• ClinVar Variation Id: 479831
• ClinVar RCV Id: RCV000575701 ; RCV003767107
• dbSNP Id: rs876660291
• MyVariant Identifiers: chr2:g.47705578A>G (hg19) ; chr2:g.47478439A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47478439A>G , CM000664.2:g.47478439A>G	GRCh38
NC_000002.11:g.47705578A>G , CM000664.1:g.47705578A>G	GRCh37
NC_000002.10:g.47559082A>G	NCBI36
NG_007110.2:g.80316A>G , LRG_218:g.80316A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2378A>G	ENSP00000495641.2:p.Gln793Arg
ENST00000233146.7:c.2378A>G MANE Select	ENSP00000233146.2:p.Gln793Arg
ENST00000543555.6:c.2180A>G	ENSP00000442697.1:p.Gln727Arg
ENST00000644092.1:c.*678A>G	ENSP00000496351.1:n.*678A>G
ENST00000644900.1:c.231A>G
ENST00000645339.1:c.2378A>G	ENSP00000496441.1:p.Gln793Arg
ENST00000645506.1:c.2378A>G	ENSP00000495455.1:p.Gln793Arg
ENST00000646415.1:c.2378A>G	ENSP00000495543.1:p.Gln793Arg
ENST00000233146.6:c.2378A>G	ENSP00000233146.2:p.Gln793Arg
ENST00000406134.5:c.2378A>G	ENSP00000384199.1:p.Gln793Arg
ENST00000543555.5:c.2180A>G	ENSP00000442697.1:p.Gln727Arg
ENST00000610696.4:c.*774A>G	ENSP00000483159.1:n.*774A>G
ENST00000613514.4:c.*918A>G	ENSP00000484137.1:n.*918A>G
ENST00000617333.3:c.*1144A>G	ENSP00000482468.1:n.*1144A>G
ENST00000617938.4:c.*1350A>G	ENSP00000481158.1:n.*1350A>G
ENST00000621359.2:c.2377A>G	ENSP00000481416.1:p.Arg793Gly
NM_000251.2:c.2378A>G , LRG_218t1:c.2378A>G	NP_000242.1:p.Gln793Arg
NM_001258281.1:c.2180A>G	NP_001245210.1:p.Gln727Arg
XM_005264332.2:c.2378A>G	XP_005264389.2:p.Gln793Arg
XM_011532867.1:c.2378A>G	XP_011531169.1:p.Gln793Arg
XR_939685.1:n.2450A>G
XM_005264332.4:c.2378A>G	XP_005264389.2:p.Gln793Arg
XM_011532867.2:c.2378A>G	XP_011531169.1:p.Gln793Arg
XR_001738747.2:n.2440A>G
XR_939685.2:n.2440A>G
NM_000251.3:c.2378A>G MANE Select	NP_000242.1:p.Gln793Arg