Canonical Allele Identifier: CA933132626

Gene: BAG3

Linked Data

• ClinVar Variation Id: 1453625
• ClinVar RCV Id: RCV001994855
• dbSNP Id: rs1847128695
• gnomAD v3: 10-119670153-GC-G
• gnomAD v4: 10-119670153-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119670158del , CM000672.2:g.119670158del	GRCh38
NC_000010.10:g.121429670del , CM000672.1:g.121429670del	GRCh37
NC_000010.9:g.121419660del	NCBI36
NG_016125.1:g.23789del , LRG_742:g.23789del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.488del MANE Select	ENSP00000358081.4:p.Pro163GlnfsTer?
ENST00000369085.7:c.488del	ENSP00000358081.3:p.Pro163GlnfsTer?
ENST00000450186.1:c.314del	ENSP00000410036.1:p.Pro105GlnfsTer?
NM_004281.3:c.488del , LRG_742t1:c.488del	NP_004272.2:p.Pro163GlnfsTer?
XM_005270287.1:c.488del	XP_005270344.1:p.Pro163GlnfsTer?
XM_005270287.2:c.488del	XP_005270344.1:p.Pro163GlnfsTer?
NM_004281.4:c.488del MANE Select	NP_004272.2:p.Pro163GlnfsTer?