Canonical Allele Identifier: CA5716438

Gene: BAG3

Linked Data

• ClinVar Variation Id: 377549
• ClinVar RCV Id: RCV000441320 ; RCV002058883 ; RCV003736756
• dbSNP Id: rs139086861
• ExAC: 10:121432185 G / A
• gnomAD v2: 10-121432185-G-A
• gnomAD v3: 10-119672673-G-A
• gnomAD v4: 10-119672673-G-A
• MyVariant Identifiers: chr10:g.121432185G>A (hg19) ; chr10:g.119672673G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119672673G>A , CM000672.2:g.119672673G>A	GRCh38
NC_000010.10:g.121432185G>A , CM000672.1:g.121432185G>A	GRCh37
NC_000010.9:g.121422175G>A	NCBI36
NG_016125.1:g.26304G>A , LRG_742:g.26304G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.909+17G>A MANE Select	ENSP00000358081.4:n.909+17G>A
ENST00000369085.7:c.909+17G>A	ENSP00000358081.3:n.909+17G>A
ENST00000450186.1:c.735+17G>A	ENSP00000410036.1:n.735+17G>A
NM_004281.3:c.909+17G>A , LRG_742t1:c.909+17G>A	NP_004272.2:n.909+17G>A
XM_005270287.1:c.909+17G>A	XP_005270344.1:n.909+17G>A
XM_005270287.2:c.909+17G>A	XP_005270344.1:n.909+17G>A
NM_004281.4:c.909+17G>A MANE Select	NP_004272.2:n.909+17G>A