Canonical Allele Identifier: CA2580067113

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1766909
• ClinVar RCV Id: RCV002373987

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47414421_47414422delinsGT , CM000664.2:g.47414421_47414422delinsGT	GRCh38
NC_000002.11:g.47641560_47641561delinsGT , CM000664.1:g.47641560_47641561delinsGT	GRCh37
NC_000002.10:g.47495064_47495065delinsGT	NCBI36
NG_007110.2:g.16298_16299delinsGT , LRG_218:g.16298_16299delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.942+3_942+4delinsGT	ENSP00000495641.2:n.942+3_942+4delinsGT
ENST00000233146.7:c.942+3_942+4delinsGT MANE Select	ENSP00000233146.2:n.942+3_942+4delinsGT
ENST00000543555.6:c.744+3_744+4delinsGT	ENSP00000442697.1:n.744+3_744+4delinsGT
ENST00000644092.1:c.942+3_942+4delinsGT	ENSP00000496351.1:n.942+3_942+4delinsGT
ENST00000645339.1:c.942+3_942+4delinsGT	ENSP00000496441.1:n.942+3_942+4delinsGT
ENST00000645506.1:c.942+3_942+4delinsGT	ENSP00000495455.1:n.942+3_942+4delinsGT
ENST00000646415.1:c.942+3_942+4delinsGT	ENSP00000495543.1:n.942+3_942+4delinsGT
ENST00000233146.6:c.942+3_942+4delinsGT	ENSP00000233146.2:n.942+3_942+4delinsGT
ENST00000406134.5:c.942+3_942+4delinsGT	ENSP00000384199.1:n.942+3_942+4delinsGT
ENST00000543555.5:c.744+3_744+4delinsGT	ENSP00000442697.1:n.744+3_744+4delinsGT
ENST00000610696.4:c.942+3_942+4delinsGT	ENSP00000483159.1:n.942+3_942+4delinsGT
ENST00000613514.4:c.942+3_942+4delinsGT	ENSP00000484137.1:n.942+3_942+4delinsGT
ENST00000617333.3:c.942+3_942+4delinsGT	ENSP00000482468.1:n.942+3_942+4delinsGT
ENST00000617938.4:c.942+3_942+4delinsGT	ENSP00000481158.1:n.942+3_942+4delinsGT
ENST00000621359.2:c.942+3_942+4delinsGT	ENSP00000481416.1:n.942+3_942+4delinsGT
NM_000251.2:c.942+3_942+4delinsGT , LRG_218t1:c.942+3_942+4delinsGT	NP_000242.1:n.942+3_942+4delinsGT
NM_001258281.1:c.744+3_744+4delinsGT	NP_001245210.1:n.744+3_744+4delinsGT
XM_005264332.2:c.942+3_942+4delinsGT	XP_005264389.2:n.942+3_942+4delinsGT
XM_011532867.1:c.942+3_942+4delinsGT	XP_011531169.1:n.942+3_942+4delinsGT
XR_939685.1:n.1014+3_1014+4delinsGT
XM_005264332.4:c.942+3_942+4delinsGT	XP_005264389.2:n.942+3_942+4delinsGT
XM_011532867.2:c.942+3_942+4delinsGT	XP_011531169.1:n.942+3_942+4delinsGT
XR_001738747.2:n.1004+3_1004+4delinsGT
XR_939685.2:n.1004+3_1004+4delinsGT
NM_000251.3:c.942+3_942+4delinsGT MANE Select	NP_000242.1:n.942+3_942+4delinsGT