Canonical Allele Identifier: CA658656095
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 471798
ClinVar RCV Id: RCV000540680
dbSNP Id: rs1554877765
MyVariant Identifiers: chr10:g.121436227dup (hg19) chr10:g.119676715dup (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676715dup , CM000672.2:g.119676715dup GRCh38
NC_000010.10:g.121436227dup , CM000672.1:g.121436227dup GRCh37
NC_000010.9:g.121426217dup NCBI36
NG_016125.1:g.30346dup , LRG_742:g.30346dup

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.1161dup MANE Select ENSP00000358081.4:p.Lys388GlnfsTer?
ENST00000369085.7:c.1161dup ENSP00000358081.3:p.Lys388GlnfsTer?
NM_004281.3:c.1161dup , LRG_742t1:c.1161dup NP_004272.2:p.Lys388GlnfsTer?
XM_005270287.1:c.1158dup XP_005270344.1:p.Lys387GlnfsTer?
XM_005270287.2:c.1158dup XP_005270344.1:p.Lys387GlnfsTer?
NM_004281.4:c.1161dup MANE Select NP_004272.2:p.Lys388GlnfsTer?
Search 100 bp 5'
Search 100 bp 3'