Canonical Allele Identifier: CA5716352

Gene: BAG3

Linked Data

• dbSNP Id: rs536339219
• ExAC: 10:121431718 CAGGGG / C
• gnomAD v2: 10-121431718-CAGGGG-C
• gnomAD v3: 10-119672206-CAGGGG-C
• gnomAD v4: 10-119672206-CAGGGG-C
• MyVariant Identifiers: chr10:g.121431719_121431723del (hg19) ; chr10:g.119672207_119672211del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119672209_119672213del , CM000672.2:g.119672209_119672213del	GRCh38
NC_000010.10:g.121431721_121431725del , CM000672.1:g.121431721_121431725del	GRCh37
NC_000010.9:g.121421711_121421715del	NCBI36
NG_016125.1:g.25840_25844del , LRG_742:g.25840_25844del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.508-46_508-42del MANE Select	ENSP00000358081.4:n.508-46_508-42del
ENST00000369085.7:c.508-46_508-42del	ENSP00000358081.3:n.508-46_508-42del
ENST00000450186.1:c.334-46_334-42del	ENSP00000410036.1:n.334-46_334-42del
NM_004281.3:c.508-46_508-42del , LRG_742t1:c.508-46_508-42del	NP_004272.2:n.508-46_508-42del
XM_005270287.1:c.508-46_508-42del	XP_005270344.1:n.508-46_508-42del
XM_005270287.2:c.508-46_508-42del	XP_005270344.1:n.508-46_508-42del
NM_004281.4:c.508-46_508-42del MANE Select	NP_004272.2:n.508-46_508-42del