Canonical Allele Identifier: CA471634625

Gene: BAG3

Linked Data

• ClinVar Variation Id: 795750
• ClinVar RCV Id: RCV001472039
• dbSNP Id: rs1589629040
• MyVariant Identifiers: chr10:g.121429683A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119670171A>G , CM000672.2:g.119670171A>G	GRCh38
NC_000010.10:g.121429683A>G , CM000672.1:g.121429683A>G	GRCh37
NC_000010.9:g.121419673A>G	NCBI36
NG_016125.1:g.23802A>G , LRG_742:g.23802A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.501A>G MANE Select	ENSP00000358081.4:p.Gly167=
ENST00000369085.7:c.501A>G	ENSP00000358081.3:p.Gly167=
ENST00000450186.1:c.327A>G	ENSP00000410036.1:p.Gly109=
NM_004281.3:c.501A>G , LRG_742t1:c.501A>G	NP_004272.2:p.Gly167=
XM_005270287.1:c.501A>G	XP_005270344.1:p.Gly167=
XM_005270287.2:c.501A>G	XP_005270344.1:p.Gly167=
NM_004281.4:c.501A>G MANE Select	NP_004272.2:p.Gly167=