Canonical Allele Identifier: CA2580082424
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1753385
ClinVar RCV Id: RCV002361628
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672388_119672414del , CM000672.2:g.119672388_119672414del GRCh38
NC_000010.10:g.121431900_121431926del , CM000672.1:g.121431900_121431926del GRCh37
NC_000010.9:g.121421890_121421916del NCBI36
NG_016125.1:g.26019_26045del , LRG_742:g.26019_26045del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.641_667del MANE Select ENSP00000358081.4:p.Gln214_Gln222del
ENST00000369085.7:c.641_667del ENSP00000358081.3:p.Gln214_Gln222del
ENST00000450186.1:c.467_493del ENSP00000410036.1:p.Gln156_Gln164del
NM_004281.3:c.641_667del , LRG_742t1:c.641_667del NP_004272.2:p.Gln214_Gln222del
XM_005270287.1:c.641_667del XP_005270344.1:p.Gln214_Gln222del
XM_005270287.2:c.641_667del XP_005270344.1:p.Gln214_Gln222del
NM_004281.4:c.641_667del MANE Select NP_004272.2:p.Gln214_Gln222del
Search 100 bp 5'
Search 100 bp 3'