Canonical Allele Identifier: CA10577925
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 233629
ClinVar RCV Id: RCV000216646
dbSNP Id: rs876660533

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47408400_47408410delinsCAC , CM000664.2:g.47408400_47408410delinsCAC GRCh38
NC_000002.11:g.47635539_47635549delinsCAC , CM000664.1:g.47635539_47635549delinsCAC GRCh37
NC_000002.10:g.47489043_47489053delinsCAC NCBI36
NG_007110.2:g.10277_10287delinsCAC , LRG_218:g.10277_10287delinsCAC

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.212-1_221delinsCAC
ENST00000233146.7:c.212-1_221delinsCAC
ENST00000543555.6:c.14-1_23delinsCAC
ENST00000644092.1:c.212-1_221delinsCAC
ENST00000645339.1:c.212-1_221delinsCAC
ENST00000645506.1:c.212-1_221delinsCAC
ENST00000646415.1:c.212-1_221delinsCAC
ENST00000233146.6:c.212-1_221delinsCAC
ENST00000406134.5:c.212-1_221delinsCAC
ENST00000454849.5:c.14-1_23delinsCAC
ENST00000543555.5:c.14-1_23delinsCAC
ENST00000610696.4:c.212-1_221delinsCAC
ENST00000613514.4:c.212-1_221delinsCAC
ENST00000617333.3:c.212-1_221delinsCAC
ENST00000617938.4:c.212-1_221delinsCAC
ENST00000621359.2:c.212-1_221delinsCAC
NM_000251.2:c.212-1_221delinsCAC , LRG_218t1:c.212-1_221delinsCAC
NM_001258281.1:c.14-1_23delinsCAC
XM_005264332.2:c.212-1_221delinsCAC
XM_011532867.1:c.212-1_221delinsCAC
XR_939685.1:n.284-1_293delinsCAC
XM_005264332.4:c.212-1_221delinsCAC
XM_011532867.2:c.212-1_221delinsCAC
XR_001738747.2:n.274-1_283delinsCAC
XR_939685.2:n.274-1_283delinsCAC
NM_000251.3:c.212-1_221delinsCAC