Canonical Allele Identifier: CA1940193164
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1847161722

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672320_119672321insTCT , CM000672.2:g.119672320_119672321insTCT GRCh38
NC_000010.10:g.121431832_121431833insTCT , CM000672.1:g.121431832_121431833insTCT GRCh37
NC_000010.9:g.121421822_121421823insTCT NCBI36
NG_016125.1:g.25951_25952insTCT , LRG_742:g.25951_25952insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.573_574insTCT MANE Select ENSP00000358081.4:p.Ser191_Gly192insSer
ENST00000369085.7:c.573_574insTCT ENSP00000358081.3:p.Ser191_Gly192insSer
ENST00000450186.1:c.399_400insTCT ENSP00000410036.1:p.Ser133_Gly134insSer
NM_004281.3:c.573_574insTCT , LRG_742t1:c.573_574insTCT NP_004272.2:p.Ser191_Gly192insSer
XM_005270287.1:c.573_574insTCT XP_005270344.1:p.Ser191_Gly192insSer
XM_005270287.2:c.573_574insTCT XP_005270344.1:p.Ser191_Gly192insSer
NM_004281.4:c.573_574insTCT MANE Select NP_004272.2:p.Ser191_Gly192insSer