Canonical Allele Identifier: CA378295017

Gene: BAG3

Linked Data

• gnomAD v4: 10-119670071-C-G
• MyVariant Identifiers: chr10:g.121429583C>G (hg19) ; chr10:g.119670071C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119670071C>G , CM000672.2:g.119670071C>G	GRCh38
NC_000010.10:g.121429583C>G , CM000672.1:g.121429583C>G	GRCh37
NC_000010.9:g.121419573C>G	NCBI36
NG_016125.1:g.23702C>G , LRG_742:g.23702C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.401C>G MANE Select	ENSP00000358081.4:p.Ser134Cys
ENST00000369085.7:c.401C>G	ENSP00000358081.3:p.Ser134Cys
ENST00000450186.1:c.227C>G	ENSP00000410036.1:p.Ser76Cys
NM_004281.3:c.401C>G , LRG_742t1:c.401C>G	NP_004272.2:p.Ser134Cys
XM_005270287.1:c.401C>G	XP_005270344.1:p.Ser134Cys
XM_005270287.2:c.401C>G	XP_005270344.1:p.Ser134Cys
NM_004281.4:c.401C>G MANE Select	NP_004272.2:p.Ser134Cys