Canonical Allele Identifier: CA16618931
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 424122
ClinVar RCV Id: RCV001228400
dbSNP Id: rs1064796808
MyVariant Identifiers: chr10:g.121411302_121411304del (hg19) chr10:g.119651790_119651792del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119651790_119651792del , CM000672.2:g.119651790_119651792del GRCh38
NC_000010.10:g.121411302_121411304del , CM000672.1:g.121411302_121411304del GRCh37
NC_000010.9:g.121401292_121401294del NCBI36
NG_016125.1:g.5421_5423del , LRG_742:g.5421_5423del

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.115_117del MANE Select ENSP00000358081.4:p.Phe39del
ENST00000369085.7:c.115_117del ENSP00000358081.3:p.Phe39del
NM_004281.3:c.115_117del , LRG_742t1:c.115_117del NP_004272.2:p.Phe39del
XM_005270287.1:c.115_117del XP_005270344.1:p.Phe39del
XM_005270287.2:c.115_117del XP_005270344.1:p.Phe39del
NM_004281.4:c.115_117del MANE Select NP_004272.2:p.Phe39del
Search 100 bp 5'
Search 100 bp 3'