Canonical Allele Identifier: CA1940193446
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2926829
ClinVar RCV Id: RCV003789067
dbSNP Id: rs1847166370
gnomAD v3: 10-119672526-TGCGGGCGGCATCCCC-T
gnomAD v4: 10-119672526-TGCGGGCGGCATCCCC-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672528_119672542del , CM000672.2:g.119672528_119672542del GRCh38
NC_000010.10:g.121432040_121432054del , CM000672.1:g.121432040_121432054del GRCh37
NC_000010.9:g.121422030_121422044del NCBI36
NG_016125.1:g.26159_26173del , LRG_742:g.26159_26173del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.781_795del MANE Select ENSP00000358081.4:p.Arg261_Pro265del
ENST00000369085.7:c.781_795del ENSP00000358081.3:p.Arg261_Pro265del
ENST00000450186.1:c.607_621del ENSP00000410036.1:p.Arg203_Pro207del
NM_004281.3:c.781_795del , LRG_742t1:c.781_795del NP_004272.2:p.Arg261_Pro265del
XM_005270287.1:c.781_795del XP_005270344.1:p.Arg261_Pro265del
XM_005270287.2:c.781_795del XP_005270344.1:p.Arg261_Pro265del
NM_004281.4:c.781_795del MANE Select NP_004272.2:p.Arg261_Pro265del
Search 100 bp 5'
Search 100 bp 3'