Canonical Allele Identifier: CA2580082414
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453001
ClinVar RCV Id: RCV003177775

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669893del , CM000672.2:g.119669893del GRCh38
NC_000010.10:g.121429405del , CM000672.1:g.121429405del GRCh37
NC_000010.9:g.121419395del NCBI36
NG_016125.1:g.23524del , LRG_742:g.23524del

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.223del MANE Select ENSP00000358081.4:p.Arg75GlyfsTer?
ENST00000369085.7:c.223del ENSP00000358081.3:p.Arg75GlyfsTer?
ENST00000450186.1:c.49del ENSP00000410036.1:p.Arg17GlyfsTer?
NM_004281.3:c.223del , LRG_742t1:c.223del NP_004272.2:p.Arg75GlyfsTer?
XM_005270287.1:c.223del XP_005270344.1:p.Arg75GlyfsTer?
XM_005270287.2:c.223del XP_005270344.1:p.Arg75GlyfsTer?
NM_004281.4:c.223del MANE Select NP_004272.2:p.Arg75GlyfsTer?