Canonical Allele Identifier: CA029000

Gene: MSH2

Linked Data

• ClinVar Variation Id: 372031
• ClinVar RCV Id: RCV000410661 ; RCV000442358 ; RCV000579684 ; RCV001356660 ; RCV002058850 ; RCV003237837
• dbSNP Id: rs370675562
• ExAC: 2:47690304 G / C
• gnomAD v2: 2-47690304-G-C
• gnomAD v3: 2-47463165-G-C
• gnomAD v4: 2-47463165-G-C
• MyVariant Identifiers: chr2:g.47690304G>C (hg19) ; chr2:g.47463165G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47463165G>C , CM000664.2:g.47463165G>C	GRCh38
NC_000002.11:g.47690304G>C , CM000664.1:g.47690304G>C	GRCh37
NC_000002.10:g.47543808G>C	NCBI36
NG_007110.2:g.65042G>C , LRG_218:g.65042G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1510+11G>C	ENSP00000495641.2:n.1510+11G>C
ENST00000233146.7:c.1510+11G>C MANE Select	ENSP00000233146.2:n.1510+11G>C
ENST00000543555.6:c.1312+11G>C	ENSP00000442697.1:n.1312+11G>C
ENST00000644092.1:c.1510+11G>C	ENSP00000496351.1:n.1510+11G>C
ENST00000645339.1:c.1510+11G>C	ENSP00000496441.1:n.1510+11G>C
ENST00000645506.1:c.1510+11G>C	ENSP00000495455.1:n.1510+11G>C
ENST00000646415.1:c.1510+11G>C	ENSP00000495543.1:n.1510+11G>C
ENST00000233146.6:c.1510+11G>C	ENSP00000233146.2:n.1510+11G>C
ENST00000406134.5:c.1510+11G>C	ENSP00000384199.1:n.1510+11G>C
ENST00000543555.5:c.1312+11G>C	ENSP00000442697.1:n.1312+11G>C
ENST00000610696.4:c.1510+11G>C	ENSP00000483159.1:n.1510+11G>C
ENST00000613514.4:c.*50+11G>C	ENSP00000484137.1:n.*50+11G>C
ENST00000617333.3:c.*276+11G>C	ENSP00000482468.1:n.*276+11G>C
ENST00000617938.4:c.*482+11G>C	ENSP00000481158.1:n.*482+11G>C
ENST00000621359.2:c.1510+11G>C	ENSP00000481416.1:n.1510+11G>C
NM_000251.2:c.1510+11G>C , LRG_218t1:c.1510+11G>C	NP_000242.1:n.1510+11G>C
NM_001258281.1:c.1312+11G>C	NP_001245210.1:n.1312+11G>C
XM_005264332.2:c.1510+11G>C	XP_005264389.2:n.1510+11G>C
XM_011532867.1:c.1510+11G>C	XP_011531169.1:n.1510+11G>C
XR_939685.1:n.1582+11G>C
XM_005264332.4:c.1510+11G>C	XP_005264389.2:n.1510+11G>C
XM_011532867.2:c.1510+11G>C	XP_011531169.1:n.1510+11G>C
XR_001738747.2:n.1572+11G>C
XR_939685.2:n.1572+11G>C
NM_000251.3:c.1510+11G>C MANE Select	NP_000242.1:n.1510+11G>C