Canonical Allele Identifier: CA2495834053

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47414418_47414420delinsGGT , CM000664.2:g.47414418_47414420delinsGGT	GRCh38
NC_000002.11:g.47641557_47641559delinsGGT , CM000664.1:g.47641557_47641559delinsGGT	GRCh37
NC_000002.10:g.47495061_47495063delinsGGT	NCBI36
NG_007110.2:g.16295_16297delinsGGT , LRG_218:g.16295_16297delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.942_942+2delinsGGT
ENST00000233146.7:c.942_942+2delinsGGT
ENST00000543555.6:c.744_744+2delinsGGT
ENST00000644092.1:c.942_942+2delinsGGT
ENST00000645339.1:c.942_942+2delinsGGT
ENST00000645506.1:c.942_942+2delinsGGT
ENST00000646415.1:c.942_942+2delinsGGT
ENST00000233146.6:c.942_942+2delinsGGT
ENST00000406134.5:c.942_942+2delinsGGT
ENST00000543555.5:c.744_744+2delinsGGT
ENST00000610696.4:c.942_942+2delinsGGT
ENST00000613514.4:c.942_942+2delinsGGT
ENST00000617333.3:c.942_942+2delinsGGT
ENST00000617938.4:c.942_942+2delinsGGT
ENST00000621359.2:c.942_942+2delinsGGT
NM_000251.2:c.942_942+2delinsGGT , LRG_218t1:c.942_942+2delinsGGT
NM_001258281.1:c.744_744+2delinsGGT
XM_005264332.2:c.942_942+2delinsGGT
XM_011532867.1:c.942_942+2delinsGGT
XR_939685.1:n.1014_1014+2delinsGGT
XM_005264332.4:c.942_942+2delinsGGT
XM_011532867.2:c.942_942+2delinsGGT
XR_001738747.2:n.1004_1004+2delinsGGT
XR_939685.2:n.1004_1004+2delinsGGT
NM_000251.3:c.942_942+2delinsGGT