Canonical Allele Identifier: CA346729111

Gene: MSH2

Linked Data

• MyVariant Identifiers: chr2:g.47703529A>C (hg19) ; chr2:g.47476390A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47476390A>C , CM000664.2:g.47476390A>C	GRCh38
NC_000002.11:g.47703529A>C , CM000664.1:g.47703529A>C	GRCh37
NC_000002.10:g.47557033A>C	NCBI36
NG_007110.2:g.78267A>C , LRG_218:g.78267A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.2029A>C	ENSP00000495641.2:p.Thr677Pro
ENST00000233146.7:c.2029A>C MANE Select	ENSP00000233146.2:p.Thr677Pro
ENST00000543555.6:c.1831A>C	ENSP00000442697.1:p.Thr611Pro
ENST00000644092.1:c.*329A>C	ENSP00000496351.1:n.*329A>C
ENST00000645339.1:c.2029A>C	ENSP00000496441.1:p.Thr677Pro
ENST00000645506.1:c.2029A>C	ENSP00000495455.1:p.Thr677Pro
ENST00000646415.1:c.2029A>C	ENSP00000495543.1:p.Thr677Pro
ENST00000233146.6:c.2029A>C	ENSP00000233146.2:p.Thr677Pro
ENST00000406134.5:c.2029A>C	ENSP00000384199.1:p.Thr677Pro
ENST00000543555.5:c.1831A>C	ENSP00000442697.1:p.Thr611Pro
ENST00000610696.4:c.*425A>C	ENSP00000483159.1:n.*425A>C
ENST00000613514.4:c.*569A>C	ENSP00000484137.1:n.*569A>C
ENST00000617333.3:c.*795A>C	ENSP00000482468.1:n.*795A>C
ENST00000617938.4:c.*1001A>C	ENSP00000481158.1:n.*1001A>C
ENST00000621359.2:c.2029A>C	ENSP00000481416.1:p.Thr677Pro
NM_000251.2:c.2029A>C , LRG_218t1:c.2029A>C	NP_000242.1:p.Thr677Pro
NM_001258281.1:c.1831A>C	NP_001245210.1:p.Thr611Pro
XM_005264332.2:c.2029A>C	XP_005264389.2:p.Thr677Pro
XM_011532867.1:c.2029A>C	XP_011531169.1:p.Thr677Pro
XR_939685.1:n.2101A>C
XM_005264332.4:c.2029A>C	XP_005264389.2:p.Thr677Pro
XM_011532867.2:c.2029A>C	XP_011531169.1:p.Thr677Pro
XR_001738747.2:n.2091A>C
XR_939685.2:n.2091A>C
NM_000251.3:c.2029A>C MANE Select	NP_000242.1:p.Thr677Pro