Canonical Allele Identifier: CA2580082468
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2106043
ClinVar RCV Id: RCV003015069
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672474dup , CM000672.2:g.119672474dup GRCh38
NC_000010.10:g.121431986dup , CM000672.1:g.121431986dup GRCh37
NC_000010.9:g.121421976dup NCBI36
NG_016125.1:g.26105dup , LRG_742:g.26105dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.727dup MANE Select ENSP00000358081.4:p.His243ProfsTer12
ENST00000369085.7:c.727dup ENSP00000358081.3:p.His243ProfsTer12
ENST00000450186.1:c.553dup ENSP00000410036.1:p.His185ProfsTer12
NM_004281.3:c.727dup , LRG_742t1:c.727dup NP_004272.2:p.His243ProfsTer12
XM_005270287.1:c.727dup XP_005270344.1:p.His243ProfsTer12
XM_005270287.2:c.727dup XP_005270344.1:p.His243ProfsTer12
NM_004281.4:c.727dup MANE Select NP_004272.2:p.His243ProfsTer12
Search 100 bp 5'
Search 100 bp 3'