Canonical Allele Identifier: CA471634843

Gene: BAG3

Linked Data

• ClinVar Variation Id: 1141519
• ClinVar RCV Id: RCV001478967
• dbSNP Id: rs2134068761
• MyVariant Identifiers: chr10:g.121436083T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119676571T>A , CM000672.2:g.119676571T>A	GRCh38
NC_000010.10:g.121436083T>A , CM000672.1:g.121436083T>A	GRCh37
NC_000010.9:g.121426073T>A	NCBI36
NG_016125.1:g.30202T>A , LRG_742:g.30202T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.1017T>A MANE Select	ENSP00000358081.4:p.Ile339=
ENST00000369085.7:c.1017T>A	ENSP00000358081.3:p.Ile339=
ENST00000450186.1:c.840T>A	ENSP00000410036.1:p.Ile280=
NM_004281.3:c.1017T>A , LRG_742t1:c.1017T>A	NP_004272.2:p.Ile339=
XM_005270287.1:c.1014T>A	XP_005270344.1:p.Ile338=
XM_005270287.2:c.1014T>A	XP_005270344.1:p.Ile338=
NM_004281.4:c.1017T>A MANE Select	NP_004272.2:p.Ile339=