Canonical Allele Identifier: CA346731771

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1795144
• ClinVar RCV Id: RCV002431246
• dbSNP Id: rs2104461311
• MyVariant Identifiers: chr2:g.47710002A>T (hg19) ; chr2:g.47482863A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47482863A>T , CM000664.2:g.47482863A>T	GRCh38
NC_000002.11:g.47710002A>T , CM000664.1:g.47710002A>T	GRCh37
NC_000002.10:g.47563506A>T	NCBI36
NG_007110.2:g.84740A>T , LRG_218:g.84740A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+1992A>T	ENSP00000495641.2:n.2634+1992A>T
ENST00000233146.7:c.2719A>T MANE Select	ENSP00000233146.2:p.Lys907Ter
ENST00000543555.6:c.2521A>T	ENSP00000442697.1:p.Lys841Ter
ENST00000644092.1:c.*934+1992A>T	ENSP00000496351.1:n.*934+1992A>T
ENST00000644900.1:c.487+1992A>T
ENST00000645339.1:c.2634+1992A>T	ENSP00000496441.1:n.2634+1992A>T
ENST00000645506.1:c.2634+1992A>T	ENSP00000495455.1:n.2634+1992A>T
ENST00000646415.1:c.2634+1992A>T	ENSP00000495543.1:n.2634+1992A>T
ENST00000233146.6:c.2719A>T	ENSP00000233146.2:p.Lys907Ter
ENST00000406134.5:c.2634+1992A>T	ENSP00000384199.1:n.2634+1992A>T
ENST00000461394.5:n.75+1992A>T
ENST00000543555.5:c.2521A>T	ENSP00000442697.1:p.Lys841Ter
ENST00000610696.4:c.*1115A>T	ENSP00000483159.1:n.*1115A>T
ENST00000613514.4:c.*1259A>T	ENSP00000484137.1:n.*1259A>T
ENST00000617333.3:c.*1485A>T	ENSP00000482468.1:n.*1485A>T
ENST00000617938.4:c.*1691A>T	ENSP00000481158.1:n.*1691A>T
ENST00000621359.2:c.*285A>T	ENSP00000481416.1:n.*285A>T
NM_000251.2:c.2719A>T , LRG_218t1:c.2719A>T	NP_000242.1:p.Lys907Ter
NM_001258281.1:c.2521A>T	NP_001245210.1:p.Lys841Ter
XM_005264332.2:c.2634+1992A>T	XP_005264389.2:n.2634+1992A>T
XM_011532867.1:c.2634+1992A>T	XP_011531169.1:n.2634+1992A>T
XR_939685.1:n.2706+1992A>T
XM_005264332.4:c.2634+1992A>T	XP_005264389.2:n.2634+1992A>T
XM_011532867.2:c.2634+1992A>T	XP_011531169.1:n.2634+1992A>T
XR_001738747.2:n.2696+1992A>T
XR_939685.2:n.2696+1992A>T
NM_000251.3:c.2719A>T MANE Select	NP_000242.1:p.Lys907Ter