Canonical Allele Identifier: CA10581154

Gene: BAG3

Linked Data

• ClinVar Variation Id: 234982
• ClinVar RCV Id: RCV000223884 ; RCV000463650 ; RCV002372238
• dbSNP Id: rs876661342
• gnomAD v4: 10-119672446-C-A
• MyVariant Identifiers: chr10:g.121431958C>A (hg19) ; chr10:g.119672446C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119672446C>A , CM000672.2:g.119672446C>A	GRCh38
NC_000010.10:g.121431958C>A , CM000672.1:g.121431958C>A	GRCh37
NC_000010.9:g.121421948C>A	NCBI36
NG_016125.1:g.26077C>A , LRG_742:g.26077C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369085.8:c.699C>A MANE Select	ENSP00000358081.4:p.Tyr233Ter
ENST00000369085.7:c.699C>A	ENSP00000358081.3:p.Tyr233Ter
ENST00000450186.1:c.525C>A	ENSP00000410036.1:p.Tyr175Ter
NM_004281.3:c.699C>A , LRG_742t1:c.699C>A	NP_004272.2:p.Tyr233Ter
XM_005270287.1:c.699C>A	XP_005270344.1:p.Tyr233Ter
XM_005270287.2:c.699C>A	XP_005270344.1:p.Tyr233Ter
NM_004281.4:c.699C>A MANE Select	NP_004272.2:p.Tyr233Ter