Canonical Allele Identifier: CA020697

Gene: MSH2

Linked Data

• ClinVar Variation Id: 182585
• ClinVar RCV Id: RCV000160621 ; RCV000168241 ; RCV000656883 ; RCV000235176 ; RCV000663089
• dbSNP Id: rs140754514
• ExAC: 2:47707913 A / G
• gnomAD v2: 2-47707913-A-G
• gnomAD v3: 2-47480774-A-G
• gnomAD v4: 2-47480774-A-G
• MyVariant Identifiers: chr2:g.47707913A>G (hg19) ; chr2:g.47480774A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480774A>G , CM000664.2:g.47480774A>G	GRCh38
NC_000002.11:g.47707913A>G , CM000664.1:g.47707913A>G	GRCh37
NC_000002.10:g.47561417A>G	NCBI36
NG_007110.2:g.82651A>G , LRG_218:g.82651A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2537A>G	ENSP00000495641.2:p.Gln846Arg
ENST00000233146.7:c.2537A>G MANE Select	ENSP00000233146.2:p.Gln846Arg
ENST00000543555.6:c.2339A>G	ENSP00000442697.1:p.Gln780Arg
ENST00000644092.1:c.*837A>G	ENSP00000496351.1:n.*837A>G
ENST00000644900.1:c.390A>G
ENST00000645339.1:c.2537A>G	ENSP00000496441.1:p.Gln846Arg
ENST00000645506.1:c.2537A>G	ENSP00000495455.1:p.Gln846Arg
ENST00000646415.1:c.2537A>G	ENSP00000495543.1:p.Gln846Arg
ENST00000233146.6:c.2537A>G	ENSP00000233146.2:p.Gln846Arg
ENST00000406134.5:c.2537A>G	ENSP00000384199.1:p.Gln846Arg
ENST00000543555.5:c.2339A>G	ENSP00000442697.1:p.Gln780Arg
ENST00000610696.4:c.*933A>G	ENSP00000483159.1:n.*933A>G
ENST00000613514.4:c.*1077A>G	ENSP00000484137.1:n.*1077A>G
ENST00000617333.3:c.*1303A>G	ENSP00000482468.1:n.*1303A>G
ENST00000617938.4:c.*1509A>G	ENSP00000481158.1:n.*1509A>G
ENST00000621359.2:c.*103A>G	ENSP00000481416.1:n.*103A>G
NM_000251.2:c.2537A>G , LRG_218t1:c.2537A>G	NP_000242.1:p.Gln846Arg
NM_001258281.1:c.2339A>G	NP_001245210.1:p.Gln780Arg
XM_005264332.2:c.2537A>G	XP_005264389.2:p.Gln846Arg
XM_011532867.1:c.2537A>G	XP_011531169.1:p.Gln846Arg
XR_939685.1:n.2609A>G
XM_005264332.4:c.2537A>G	XP_005264389.2:p.Gln846Arg
XM_011532867.2:c.2537A>G	XP_011531169.1:p.Gln846Arg
XR_001738747.2:n.2599A>G
XR_939685.2:n.2599A>G
NM_000251.3:c.2537A>G MANE Select	NP_000242.1:p.Gln846Arg