Canonical Allele Identifier: CA378294717

Gene: BAG3

Linked Data

• gnomAD v4: 10-119669915-G-A
• MyVariant Identifiers: chr10:g.121429427G>A (hg19) ; chr10:g.119669915G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119669915G>A , CM000672.2:g.119669915G>A	GRCh38
NC_000010.10:g.121429427G>A , CM000672.1:g.121429427G>A	GRCh37
NC_000010.9:g.121419417G>A	NCBI36
NG_016125.1:g.23546G>A , LRG_742:g.23546G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.245G>A MANE Select	ENSP00000358081.4:p.Gly82Asp
ENST00000369085.7:c.245G>A	ENSP00000358081.3:p.Gly82Asp
ENST00000450186.1:c.71G>A	ENSP00000410036.1:p.Gly24Asp
NM_004281.3:c.245G>A , LRG_742t1:c.245G>A	NP_004272.2:p.Gly82Asp
XM_005270287.1:c.245G>A	XP_005270344.1:p.Gly82Asp
XM_005270287.2:c.245G>A	XP_005270344.1:p.Gly82Asp
NM_004281.4:c.245G>A MANE Select	NP_004272.2:p.Gly82Asp