Canonical Allele Identifier: CA660664701
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1206891717
gnomAD v3: 10-119672194-AG-A
gnomAD v4: 10-119672194-AG-A
MyVariant Identifiers: chr10:g.121431707del (hg19) chr10:g.119672195del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672196del , CM000672.2:g.119672196del GRCh38
NC_000010.10:g.121431708del , CM000672.1:g.121431708del GRCh37
NC_000010.9:g.121421698del NCBI36
NG_016125.1:g.25827del , LRG_742:g.25827del

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.508-59del MANE Select ENSP00000358081.4:n.508-59del
ENST00000369085.7:c.508-59del ENSP00000358081.3:n.508-59del
ENST00000450186.1:c.334-59del ENSP00000410036.1:n.334-59del
NM_004281.3:c.508-59del , LRG_742t1:c.508-59del NP_004272.2:n.508-59del
XM_005270287.1:c.508-59del XP_005270344.1:n.508-59del
XM_005270287.2:c.508-59del XP_005270344.1:n.508-59del
NM_004281.4:c.508-59del MANE Select NP_004272.2:n.508-59del
Search 100 bp 5'
Search 100 bp 3'