Canonical Allele Identifier: CA5716359

Gene: BAG3

Linked Data

• ClinVar Variation Id: 429486
• ClinVar RCV Id: RCV000493885 ; RCV000648835 ; RCV002350100
• dbSNP Id: rs140904592
• ExAC: 10:121431768 G / A
• gnomAD v2: 10-121431768-G-A
• gnomAD v3: 10-119672256-G-A
• gnomAD v4: 10-119672256-G-A
• MyVariant Identifiers: chr10:g.121431768G>A (hg19) ; chr10:g.119672256G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119672256G>A , CM000672.2:g.119672256G>A	GRCh38
NC_000010.10:g.121431768G>A , CM000672.1:g.121431768G>A	GRCh37
NC_000010.9:g.121421758G>A	NCBI36
NG_016125.1:g.25887G>A , LRG_742:g.25887G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.509G>A MANE Select	ENSP00000358081.4:p.Arg170Gln
ENST00000369085.7:c.509G>A	ENSP00000358081.3:p.Arg170Gln
ENST00000450186.1:c.335G>A	ENSP00000410036.1:p.Arg112Gln
NM_004281.3:c.509G>A , LRG_742t1:c.509G>A	NP_004272.2:p.Arg170Gln
XM_005270287.1:c.509G>A	XP_005270344.1:p.Arg170Gln
XM_005270287.2:c.509G>A	XP_005270344.1:p.Arg170Gln
NM_004281.4:c.509G>A MANE Select	NP_004272.2:p.Arg170Gln