Canonical Allele Identifier: CA660673444
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1174316305
gnomAD v3: 10-119669692-TG-T
gnomAD v4: 10-119669692-TG-T
MyVariant Identifiers: chr10:g.121429205del (hg19) chr10:g.119669693del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119669698del , CM000672.2:g.119669698del GRCh38
NC_000010.10:g.121429210del , CM000672.1:g.121429210del GRCh37
NC_000010.9:g.121419200del NCBI36
NG_016125.1:g.23329del , LRG_742:g.23329del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.181-153del MANE Select ENSP00000358081.4:n.181-153del
ENST00000369085.7:c.181-153del ENSP00000358081.3:n.181-153del
ENST00000450186.1:c.7-153del ENSP00000410036.1:n.7-153del
NM_004281.3:c.181-153del , LRG_742t1:c.181-153del NP_004272.2:n.181-153del
XM_005270287.1:c.181-153del XP_005270344.1:n.181-153del
XM_005270287.2:c.181-153del XP_005270344.1:n.181-153del
NM_004281.4:c.181-153del MANE Select NP_004272.2:n.181-153del
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