Canonical Allele Identifier: CA378297325

Gene: BAG3

Linked Data

• ClinVar Variation Id: 2954137
• ClinVar RCV Id: RCV003813360
• MyVariant Identifiers: chr10:g.121436508G>C (hg19) ; chr10:g.119676996G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119676996G>C , CM000672.2:g.119676996G>C	GRCh38
NC_000010.10:g.121436508G>C , CM000672.1:g.121436508G>C	GRCh37
NC_000010.9:g.121426498G>C	NCBI36
NG_016125.1:g.30627G>C , LRG_742:g.30627G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.1442G>C MANE Select	ENSP00000358081.4:p.Arg481Thr
ENST00000369085.7:c.1442G>C	ENSP00000358081.3:p.Arg481Thr
NM_004281.3:c.1442G>C , LRG_742t1:c.1442G>C	NP_004272.2:p.Arg481Thr
XM_005270287.1:c.1439G>C	XP_005270344.1:p.Arg480Thr
XM_005270287.2:c.1439G>C	XP_005270344.1:p.Arg480Thr
NM_004281.4:c.1442G>C MANE Select	NP_004272.2:p.Arg481Thr