Canonical Allele Identifier: CA2573145588
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1494973
ClinVar RCV Id: RCV001989686
dbSNP Id: rs2134068860

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676642_119677262del , CM000672.2:g.119676642_119677262del GRCh38
NC_000010.10:g.121436154_121436774del , CM000672.1:g.121436154_121436774del GRCh37
NC_000010.9:g.121426144_121426764del NCBI36
NG_016125.1:g.30273_30893del , LRG_742:g.30273_30893del

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.1088_1708del MANE Select ENSP00000358081.4:p.Glu363_Pro569del
ENST00000369085.7:c.1088_1708del ENSP00000358081.3:p.Glu363_Pro569del
NM_004281.3:c.1088_1708del , LRG_742t1:c.1088_1708del NP_004272.2:p.Glu363_Pro569del
XM_005270287.1:c.1085_1705del XP_005270344.1:p.Glu362_Pro568del
XM_005270287.2:c.1085_1705del XP_005270344.1:p.Glu362_Pro568del
NM_004281.4:c.1088_1708del MANE Select NP_004272.2:p.Glu363_Pro569del