Canonical Allele Identifier: CA1139656929
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47408401_47408408del , CM000664.2:g.47408401_47408408del GRCh38
NC_000002.11:g.47635540_47635547del , CM000664.1:g.47635540_47635547del GRCh37
NC_000002.10:g.47489044_47489051del NCBI36
NG_007110.2:g.10278_10285del , LRG_218:g.10278_10285del

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.212_219del
ENST00000233146.7:c.212_219del
ENST00000543555.6:c.14_21del
ENST00000644092.1:c.212_219del
ENST00000645339.1:c.212_219del
ENST00000645506.1:c.212_219del
ENST00000646415.1:c.212_219del
ENST00000233146.6:c.212_219del
ENST00000406134.5:c.212_219del
ENST00000454849.5:c.14_21del
ENST00000543555.5:c.14_21del
ENST00000610696.4:c.212_219del
ENST00000613514.4:c.212_219del
ENST00000617333.3:c.212_219del
ENST00000617938.4:c.212_219del
ENST00000621359.2:c.212_219del
NM_000251.2:c.212_219del , LRG_218t1:c.212_219del
NM_001258281.1:c.14_21del
XM_005264332.2:c.212_219del
XM_011532867.1:c.212_219del
XR_939685.1:n.284_291del
XM_005264332.4:c.212_219del
XM_011532867.2:c.212_219del
XR_001738747.2:n.274_281del
XR_939685.2:n.274_281del
NM_000251.3:c.212_219del