Canonical Allele Identifier: CA378293981

Gene: BAG3

Linked Data

• gnomAD v4: 10-119651683-C-T
• MyVariant Identifiers: chr10:g.121411195C>T (hg19) ; chr10:g.119651683C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119651683C>T , CM000672.2:g.119651683C>T	GRCh38
NC_000010.10:g.121411195C>T , CM000672.1:g.121411195C>T	GRCh37
NC_000010.9:g.121401185C>T	NCBI36
NG_016125.1:g.5314C>T , LRG_742:g.5314C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369085.8:c.8C>T MANE Select	ENSP00000358081.4:p.Ala3Val
ENST00000369085.7:c.8C>T	ENSP00000358081.3:p.Ala3Val
NM_004281.3:c.8C>T , LRG_742t1:c.8C>T	NP_004272.2:p.Ala3Val
XM_005270287.1:c.8C>T	XP_005270344.1:p.Ala3Val
XM_005270287.2:c.8C>T	XP_005270344.1:p.Ala3Val
NM_004281.4:c.8C>T MANE Select	NP_004272.2:p.Ala3Val