Canonical Allele Identifier: CA378294727

Gene: BAG3

Linked Data

• ClinVar Variation Id: 2094437
• ClinVar RCV Id: RCV003021338
• MyVariant Identifiers: chr10:g.121429433C>G (hg19) ; chr10:g.119669921C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119669921C>G , CM000672.2:g.119669921C>G	GRCh38
NC_000010.10:g.121429433C>G , CM000672.1:g.121429433C>G	GRCh37
NC_000010.9:g.121419423C>G	NCBI36
NG_016125.1:g.23552C>G , LRG_742:g.23552C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.251C>G MANE Select	ENSP00000358081.4:p.Pro84Arg
ENST00000369085.7:c.251C>G	ENSP00000358081.3:p.Pro84Arg
ENST00000450186.1:c.77C>G	ENSP00000410036.1:p.Pro26Arg
NM_004281.3:c.251C>G , LRG_742t1:c.251C>G	NP_004272.2:p.Pro84Arg
XM_005270287.1:c.251C>G	XP_005270344.1:p.Pro84Arg
XM_005270287.2:c.251C>G	XP_005270344.1:p.Pro84Arg
NM_004281.4:c.251C>G MANE Select	NP_004272.2:p.Pro84Arg