Canonical Allele Identifier: CA346728887

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1783863
• ClinVar RCV Id: RCV002423735
• MyVariant Identifiers: chr2:g.47702389A>G (hg19) ; chr2:g.47475250A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475250A>G , CM000664.2:g.47475250A>G	GRCh38
NC_000002.11:g.47702389A>G , CM000664.1:g.47702389A>G	GRCh37
NC_000002.10:g.47555893A>G	NCBI36
NG_007110.2:g.77127A>G , LRG_218:g.77127A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1985A>G	ENSP00000495641.2:p.Gln662Arg
ENST00000233146.7:c.1985A>G MANE Select	ENSP00000233146.2:p.Gln662Arg
ENST00000543555.6:c.1787A>G	ENSP00000442697.1:p.Gln596Arg
ENST00000644092.1:c.*285A>G	ENSP00000496351.1:n.*285A>G
ENST00000645339.1:c.1985A>G	ENSP00000496441.1:p.Gln662Arg
ENST00000645506.1:c.1985A>G	ENSP00000495455.1:p.Gln662Arg
ENST00000646415.1:c.1985A>G	ENSP00000495543.1:p.Gln662Arg
ENST00000233146.6:c.1985A>G	ENSP00000233146.2:p.Gln662Arg
ENST00000406134.5:c.1985A>G	ENSP00000384199.1:p.Gln662Arg
ENST00000543555.5:c.1787A>G	ENSP00000442697.1:p.Gln596Arg
ENST00000610696.4:c.*381A>G	ENSP00000483159.1:n.*381A>G
ENST00000613514.4:c.*525A>G	ENSP00000484137.1:n.*525A>G
ENST00000617333.3:c.*751A>G	ENSP00000482468.1:n.*751A>G
ENST00000617938.4:c.*957A>G	ENSP00000481158.1:n.*957A>G
ENST00000621359.2:c.1985A>G	ENSP00000481416.1:p.Gln662Arg
NM_000251.2:c.1985A>G , LRG_218t1:c.1985A>G	NP_000242.1:p.Gln662Arg
NM_001258281.1:c.1787A>G	NP_001245210.1:p.Gln596Arg
XM_005264332.2:c.1985A>G	XP_005264389.2:p.Gln662Arg
XM_011532867.1:c.1985A>G	XP_011531169.1:p.Gln662Arg
XR_939685.1:n.2057A>G
XM_005264332.4:c.1985A>G	XP_005264389.2:p.Gln662Arg
XM_011532867.2:c.1985A>G	XP_011531169.1:p.Gln662Arg
XR_001738747.2:n.2047A>G
XR_939685.2:n.2047A>G
NM_000251.3:c.1985A>G MANE Select	NP_000242.1:p.Gln662Arg