Canonical Allele Identifier: CA2580067110

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1791591
• ClinVar RCV Id: RCV002455467

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480696del , CM000664.2:g.47480696del	GRCh38
NC_000002.11:g.47707835del , CM000664.1:g.47707835del	GRCh37
NC_000002.10:g.47561339del	NCBI36
NG_007110.2:g.82573del , LRG_218:g.82573del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2459del
ENST00000233146.7:c.2459del
ENST00000543555.6:c.2261del
ENST00000644092.1:c.*759del
ENST00000644900.1:c.312del
ENST00000645339.1:c.2459del
ENST00000645506.1:c.2459del
ENST00000646415.1:c.2459del
ENST00000233146.6:c.2459del
ENST00000406134.5:c.2459del
ENST00000543555.5:c.2261del
ENST00000610696.4:c.*855del
ENST00000613514.4:c.*999del
ENST00000617333.3:c.*1225del
ENST00000617938.4:c.*1431del
ENST00000621359.2:c.*25del
NM_000251.2:c.2459del , LRG_218t1:c.2459del
NM_001258281.1:c.2261del
XM_005264332.2:c.2459del
XM_011532867.1:c.2459del
XR_939685.1:n.2531del
XM_005264332.4:c.2459del
XM_011532867.2:c.2459del
XR_001738747.2:n.2521del
XR_939685.2:n.2521del
NM_000251.3:c.2459del