Canonical Allele Identifier: CA214207878

Gene: BAG3

Linked Data

• dbSNP Id: rs1044507337
• gnomAD v2: 10-121411140-GAGCCAGCGCCCCGC-G
• gnomAD v3: 10-119651628-GAGCCAGCGCCCCGC-G
• gnomAD v4: 10-119651628-GAGCCAGCGCCCCGC-G
• MyVariant Identifiers: chr10:g.121411141_121411154del (hg19) ; chr10:g.119651629_119651642del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119651630_119651643del , CM000672.2:g.119651630_119651643del	GRCh38
NC_000010.10:g.121411142_121411155del , CM000672.1:g.121411142_121411155del	GRCh37
NC_000010.9:g.121401132_121401145del	NCBI36
NG_016125.1:g.5261_5274del , LRG_742:g.5261_5274del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369085.8:c.-46_-33del MANE Select	ENSP00000358081.4:n.-46_-33del
ENST00000369085.7:c.-46_-33del	ENSP00000358081.3:n.-46_-33del
NM_004281.3:c.-46_-33del , LRG_742t1:c.-46_-33del	NP_004272.2:n.-46_-33del
XM_005270287.1:c.-46_-33del	XP_005270344.1:n.-46_-33del
XM_005270287.2:c.-46_-33del	XP_005270344.1:n.-46_-33del
NM_004281.4:c.-46_-33del MANE Select	NP_004272.2:n.-46_-33del