Canonical Allele Identifier: CA471740165

Gene: BAG3

Linked Data

• ClinVar Variation Id: 3223778
• ClinVar RCV Id: RCV004516542
• MyVariant Identifiers: chr10:g.121432057C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119672545C>T , CM000672.2:g.119672545C>T	GRCh38
NC_000010.10:g.121432057C>T , CM000672.1:g.121432057C>T	GRCh37
NC_000010.9:g.121422047C>T	NCBI36
NG_016125.1:g.26176C>T , LRG_742:g.26176C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.798C>T MANE Select	ENSP00000358081.4:p.Phe266=
ENST00000369085.7:c.798C>T	ENSP00000358081.3:p.Phe266=
ENST00000450186.1:c.624C>T	ENSP00000410036.1:p.Phe208=
NM_004281.3:c.798C>T , LRG_742t1:c.798C>T	NP_004272.2:p.Phe266=
XM_005270287.1:c.798C>T	XP_005270344.1:p.Phe266=
XM_005270287.2:c.798C>T	XP_005270344.1:p.Phe266=
NM_004281.4:c.798C>T MANE Select	NP_004272.2:p.Phe266=