Canonical Allele Identifier: CA923726207
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1805453
ClinVar RCV Id: RCV002471871
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672648_119672649del , CM000672.2:g.119672648_119672649del GRCh38
NC_000010.10:g.121432160_121432161del , CM000672.1:g.121432160_121432161del GRCh37
NC_000010.9:g.121422150_121422151del NCBI36
NG_016125.1:g.26279_26280del , LRG_742:g.26279_26280del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.901_902del MANE Select ENSP00000358081.4:p.Arg301AlafsTer17
ENST00000369085.7:c.901_902del ENSP00000358081.3:p.Arg301AlafsTer17
ENST00000450186.1:c.727_728del ENSP00000410036.1:p.Arg243AlafsTer16
NM_004281.3:c.901_902del , LRG_742t1:c.901_902del NP_004272.2:p.Arg301AlafsTer17
XM_005270287.1:c.901_902del XP_005270344.1:p.Arg301AlafsTer16
XM_005270287.2:c.901_902del XP_005270344.1:p.Arg301AlafsTer16
NM_004281.4:c.901_902del MANE Select NP_004272.2:p.Arg301AlafsTer17
Search 100 bp 5'
Search 100 bp 3'