Canonical Allele Identifier: CA2580082438

Gene: BAG3

Linked Data

• ClinVar Variation Id: 1769203
• ClinVar RCV Id: RCV002380641

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119676850_119676852delinsGCG , CM000672.2:g.119676850_119676852delinsGCG	GRCh38
NC_000010.10:g.121436362_121436364delinsGCG , CM000672.1:g.121436362_121436364delinsGCG	GRCh37
NC_000010.9:g.121426352_121426354delinsGCG	NCBI36
NG_016125.1:g.30481_30483delinsGCG , LRG_742:g.30481_30483delinsGCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000369085.8:c.1296_1298delinsGCG MANE Select	ENSP00000358081.4:p.Gln433Arg
ENST00000369085.7:c.1296_1298delinsGCG	ENSP00000358081.3:p.Gln433Arg
NM_004281.3:c.1296_1298delinsGCG , LRG_742t1:c.1296_1298delinsGCG	NP_004272.2:p.Gln433Arg
XM_005270287.1:c.1293_1295delinsGCG	XP_005270344.1:p.Gln432Arg
XM_005270287.2:c.1293_1295delinsGCG	XP_005270344.1:p.Gln432Arg
NM_004281.4:c.1296_1298delinsGCG MANE Select	NP_004272.2:p.Gln433Arg