Canonical Allele Identifier: CA5716430
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 386339
dbSNP Id: rs151335530
COSMIC: COSM915384

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672628G>A , CM000672.2:g.119672628G>A GRCh38
NC_000010.10:g.121432140G>A , CM000672.1:g.121432140G>A GRCh37
NC_000010.9:g.121422130G>A NCBI36
NG_016125.1:g.26259G>A , LRG_742:g.26259G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.881G>A MANE Select ENSP00000358081.4:p.Arg294His
ENST00000369085.7:c.881G>A ENSP00000358081.3:p.Arg294His
ENST00000450186.1:c.707G>A ENSP00000410036.1:p.Arg236His
NM_004281.3:c.881G>A , LRG_742t1:c.881G>A NP_004272.2:p.Arg294His
XM_005270287.1:c.881G>A XP_005270344.1:p.Arg294His
XM_005270287.2:c.881G>A XP_005270344.1:p.Arg294His
NM_004281.4:c.881G>A MANE Select NP_004272.2:p.Arg294His