Canonical Allele Identifier: CA5716267

Gene: BAG3

Linked Data

• ClinVar Variation Id: 509096
• ClinVar RCV Id: RCV001707755 ; RCV001797760 ; RCV002420602
• dbSNP Id: rs35434411
• ExAC: 10:121429394 G / T
• gnomAD v2: 10-121429394-G-T
• gnomAD v3: 10-119669882-G-T
• gnomAD v4: 10-119669882-G-T
• MyVariant Identifiers: chr10:g.121429394G>T (hg19) ; chr10:g.119669882G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119669882G>T , CM000672.2:g.119669882G>T	GRCh38
NC_000010.10:g.121429394G>T , CM000672.1:g.121429394G>T	GRCh37
NC_000010.9:g.121419384G>T	NCBI36
NG_016125.1:g.23513G>T , LRG_742:g.23513G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369085.8:c.212G>T MANE Select	ENSP00000358081.4:p.Arg71Leu
ENST00000369085.7:c.212G>T	ENSP00000358081.3:p.Arg71Leu
ENST00000450186.1:c.38G>T	ENSP00000410036.1:p.Arg13Leu
NM_004281.3:c.212G>T , LRG_742t1:c.212G>T	NP_004272.2:p.Arg71Leu
XM_005270287.1:c.212G>T	XP_005270344.1:p.Arg71Leu
XM_005270287.2:c.212G>T	XP_005270344.1:p.Arg71Leu
NM_004281.4:c.212G>T MANE Select	NP_004272.2:p.Arg71Leu