Canonical Allele Identifier: CA16612935

Gene: BAG3

Linked Data

• ClinVar Variation Id: 410229
• ClinVar RCV Id: RCV000467242 ; RCV001384911 ; RCV002356687
• dbSNP Id: rs1554877224
• MyVariant Identifiers: chr10:g.121431866dupC (hg19) ; chr10:g.119672354dupC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119672354dup , CM000672.2:g.119672354dup	GRCh38
NC_000010.10:g.121431866dup , CM000672.1:g.121431866dup	GRCh37
NC_000010.9:g.121421856dup	NCBI36
NG_016125.1:g.25985dup , LRG_742:g.25985dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.607dup MANE Select	ENSP00000358081.4:p.Arg203ProfsTer?
ENST00000369085.7:c.607dup	ENSP00000358081.3:p.Arg203ProfsTer?
ENST00000450186.1:c.433dup	ENSP00000410036.1:p.Arg145ProfsTer?
NM_004281.3:c.607dup , LRG_742t1:c.607dup	NP_004272.2:p.Arg203ProfsTer?
XM_005270287.1:c.607dup	XP_005270344.1:p.Arg203ProfsTer?
XM_005270287.2:c.607dup	XP_005270344.1:p.Arg203ProfsTer?
NM_004281.4:c.607dup MANE Select	NP_004272.2:p.Arg203ProfsTer?