Canonical Allele Identifier: CA378296071

Gene: BAG3

Linked Data

• ClinVar Variation Id: 2927467
• ClinVar RCV Id: RCV003784097
• gnomAD v4: 10-119672631-T-G
• MyVariant Identifiers: chr10:g.121432143T>G (hg19) ; chr10:g.119672631T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119672631T>G , CM000672.2:g.119672631T>G	GRCh38
NC_000010.10:g.121432143T>G , CM000672.1:g.121432143T>G	GRCh37
NC_000010.9:g.121422133T>G	NCBI36
NG_016125.1:g.26262T>G , LRG_742:g.26262T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.884T>G MANE Select	ENSP00000358081.4:p.Val295Gly
ENST00000369085.7:c.884T>G	ENSP00000358081.3:p.Val295Gly
ENST00000450186.1:c.710T>G	ENSP00000410036.1:p.Val237Gly
NM_004281.3:c.884T>G , LRG_742t1:c.884T>G	NP_004272.2:p.Val295Gly
XM_005270287.1:c.884T>G	XP_005270344.1:p.Val295Gly
XM_005270287.2:c.884T>G	XP_005270344.1:p.Val295Gly
NM_004281.4:c.884T>G MANE Select	NP_004272.2:p.Val295Gly