Canonical Allele Identifier: CA2580067067

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1791566
• ClinVar RCV Id: RCV002455458

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47478521dup , CM000664.2:g.47478521dup	GRCh38
NC_000002.11:g.47705660dup , CM000664.1:g.47705660dup	GRCh37
NC_000002.10:g.47559164dup	NCBI36
NG_007110.2:g.80398dup , LRG_218:g.80398dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2458+2dup	ENSP00000495641.2:n.2458+2dup
ENST00000233146.7:c.2458+2dup MANE Select	ENSP00000233146.2:n.2458+2dup
ENST00000543555.6:c.2260+2dup	ENSP00000442697.1:n.2260+2dup
ENST00000644092.1:c.*758+2dup	ENSP00000496351.1:n.*758+2dup
ENST00000644900.1:c.311+2dup
ENST00000645339.1:c.2458+2dup	ENSP00000496441.1:n.2458+2dup
ENST00000645506.1:c.2458+2dup	ENSP00000495455.1:n.2458+2dup
ENST00000646415.1:c.2458+2dup	ENSP00000495543.1:n.2458+2dup
ENST00000233146.6:c.2458+2dup	ENSP00000233146.2:n.2458+2dup
ENST00000406134.5:c.2458+2dup	ENSP00000384199.1:n.2458+2dup
ENST00000543555.5:c.2260+2dup	ENSP00000442697.1:n.2260+2dup
ENST00000610696.4:c.*854+2dup	ENSP00000483159.1:n.*854+2dup
ENST00000613514.4:c.*998+2dup	ENSP00000484137.1:n.*998+2dup
ENST00000617333.3:c.*1224+2dup	ENSP00000482468.1:n.*1224+2dup
ENST00000617938.4:c.*1430+2dup	ENSP00000481158.1:n.*1430+2dup
ENST00000621359.2:c.*24+2dup	ENSP00000481416.1:n.*24+2dup
NM_000251.2:c.2458+2dup , LRG_218t1:c.2458+2dup	NP_000242.1:n.2458+2dup
NM_001258281.1:c.2260+2dup	NP_001245210.1:n.2260+2dup
XM_005264332.2:c.2458+2dup	XP_005264389.2:n.2458+2dup
XM_011532867.1:c.2458+2dup	XP_011531169.1:n.2458+2dup
XR_939685.1:n.2530+2dup
XM_005264332.4:c.2458+2dup	XP_005264389.2:n.2458+2dup
XM_011532867.2:c.2458+2dup	XP_011531169.1:n.2458+2dup
XR_001738747.2:n.2520+2dup
XR_939685.2:n.2520+2dup
NM_000251.3:c.2458+2dup MANE Select	NP_000242.1:n.2458+2dup