Canonical Allele Identifier: CA346730060

Gene: MSH2

Linked Data

• ClinVar Variation Id: 801209
• ClinVar RCV Id: RCV000985802
• dbSNP Id: rs1341247425
• MyVariant Identifiers: chr2:g.47705571G>C (hg19) ; chr2:g.47478432G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47478432G>C , CM000664.2:g.47478432G>C	GRCh38
NC_000002.11:g.47705571G>C , CM000664.1:g.47705571G>C	GRCh37
NC_000002.10:g.47559075G>C	NCBI36
NG_007110.2:g.80309G>C , LRG_218:g.80309G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2371G>C	ENSP00000495641.2:p.Ala791Pro
ENST00000233146.7:c.2371G>C MANE Select	ENSP00000233146.2:p.Ala791Pro
ENST00000543555.6:c.2173G>C	ENSP00000442697.1:p.Ala725Pro
ENST00000644092.1:c.*671G>C	ENSP00000496351.1:n.*671G>C
ENST00000644900.1:c.224G>C
ENST00000645339.1:c.2371G>C	ENSP00000496441.1:p.Ala791Pro
ENST00000645506.1:c.2371G>C	ENSP00000495455.1:p.Ala791Pro
ENST00000646415.1:c.2371G>C	ENSP00000495543.1:p.Ala791Pro
ENST00000233146.6:c.2371G>C	ENSP00000233146.2:p.Ala791Pro
ENST00000406134.5:c.2371G>C	ENSP00000384199.1:p.Ala791Pro
ENST00000543555.5:c.2173G>C	ENSP00000442697.1:p.Ala725Pro
ENST00000610696.4:c.*767G>C	ENSP00000483159.1:n.*767G>C
ENST00000613514.4:c.*911G>C	ENSP00000484137.1:n.*911G>C
ENST00000617333.3:c.*1137G>C	ENSP00000482468.1:n.*1137G>C
ENST00000617938.4:c.*1343G>C	ENSP00000481158.1:n.*1343G>C
ENST00000621359.2:c.2370G>C	ENSP00000481416.1:p.Trp790Cys
NM_000251.2:c.2371G>C , LRG_218t1:c.2371G>C	NP_000242.1:p.Ala791Pro
NM_001258281.1:c.2173G>C	NP_001245210.1:p.Ala725Pro
XM_005264332.2:c.2371G>C	XP_005264389.2:p.Ala791Pro
XM_011532867.1:c.2371G>C	XP_011531169.1:p.Ala791Pro
XR_939685.1:n.2443G>C
XM_005264332.4:c.2371G>C	XP_005264389.2:p.Ala791Pro
XM_011532867.2:c.2371G>C	XP_011531169.1:p.Ala791Pro
XR_001738747.2:n.2433G>C
XR_939685.2:n.2433G>C
NM_000251.3:c.2371G>C MANE Select	NP_000242.1:p.Ala791Pro