Canonical Allele Identifier: CA10577929

Gene: MSH2

Linked Data

• ClinVar Variation Id: 232406
• ClinVar RCV Id: RCV000215101 ; RCV000227027 ; RCV001030705 ; RCV001532987 ; RCV003997972
• dbSNP Id: rs876659747
• gnomAD v2: 2-47635594-T-C
• gnomAD v3: 2-47408455-T-C
• gnomAD v4: 2-47408455-T-C
• MyVariant Identifiers: chr2:g.47635594T>C (hg19) ; chr2:g.47408455T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47408455T>C , CM000664.2:g.47408455T>C	GRCh38
NC_000002.11:g.47635594T>C , CM000664.1:g.47635594T>C	GRCh37
NC_000002.10:g.47489098T>C	NCBI36
NG_007110.2:g.10332T>C , LRG_218:g.10332T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.266T>C	ENSP00000495641.2:p.Val89Ala
ENST00000233146.7:c.266T>C MANE Select	ENSP00000233146.2:p.Val89Ala
ENST00000543555.6:c.68T>C	ENSP00000442697.1:p.Val23Ala
ENST00000644092.1:c.266T>C	ENSP00000496351.1:p.Val89Ala
ENST00000645339.1:c.266T>C	ENSP00000496441.1:p.Val89Ala
ENST00000645506.1:c.266T>C	ENSP00000495455.1:p.Val89Ala
ENST00000646415.1:c.266T>C	ENSP00000495543.1:p.Val89Ala
ENST00000233146.6:c.266T>C	ENSP00000233146.2:p.Val89Ala
ENST00000406134.5:c.266T>C	ENSP00000384199.1:p.Val89Ala
ENST00000454849.5:c.68T>C	ENSP00000411482.1:p.Val23Ala
ENST00000543555.5:c.68T>C	ENSP00000442697.1:p.Val23Ala
ENST00000610696.4:c.266T>C	ENSP00000483159.1:p.Val89Ala
ENST00000613514.4:c.266T>C	ENSP00000484137.1:p.Val89Ala
ENST00000617333.3:c.266T>C	ENSP00000482468.1:p.Val89Ala
ENST00000617938.4:c.266T>C	ENSP00000481158.1:p.Val89Ala
ENST00000621359.2:c.266T>C	ENSP00000481416.1:p.Val89Ala
NM_000251.2:c.266T>C , LRG_218t1:c.266T>C	NP_000242.1:p.Val89Ala
NM_001258281.1:c.68T>C	NP_001245210.1:p.Val23Ala
XM_005264332.2:c.266T>C	XP_005264389.2:p.Val89Ala
XM_011532867.1:c.266T>C	XP_011531169.1:p.Val89Ala
XR_939685.1:n.338T>C
XM_005264332.4:c.266T>C	XP_005264389.2:p.Val89Ala
XM_011532867.2:c.266T>C	XP_011531169.1:p.Val89Ala
XR_001738747.2:n.328T>C
XR_939685.2:n.328T>C
NM_000251.3:c.266T>C MANE Select	NP_000242.1:p.Val89Ala