Canonical Allele Identifier: CA3718061

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs745781412
• ExAC: 6:31625818 CT / C
• gnomAD v2: 6-31625818-CT-C
• gnomAD v4: 6-31658041-CT-C
• MyVariant Identifiers: chr6:g.31625819del (hg19) ; chr6:g.31658042del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658046del , CM000668.2:g.31658046del	GRCh38
NC_000006.11:g.31625823del , CM000668.1:g.31625823del	GRCh37
NC_000006.10:g.31733802del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.542-18del (APOM) MANE Select	ENSP00000365081.3:n.542-18del
ENST00000375916.3:c.542-18del (APOM)	ENSP00000365081.3:n.542-18del
ENST00000375918.6:c.*258del (APOM)	ENSP00000365083.2:n.*258del
ENST00000375920.8:c.326-18del (APOM)	ENSP00000365085.4:n.326-18del
NM_001256169.1:c.326-18del (APOM)	NP_001243098.1:n.326-18del
NM_019101.2:c.542-18del (APOM)	NP_061974.2:n.542-18del
NR_045828.1:n.577-18del (APOM)
XM_006715150.2:c.446-18del (APOM)	XP_006715213.1:n.446-18del
XM_011514895.1:c.-14+2279del (BAG6)	XP_011513197.1:n.-14+2279del
XM_006715150.3:c.446-18del (APOM)	XP_006715213.1:n.446-18del
XM_017011279.2:c.-14+2279del (BAG6)	XP_016866768.1:n.-14+2279del
NM_019101.3:c.542-18del (APOM) MANE Select	NP_061974.2:n.542-18del
NM_001256169.2:c.326-18del (APOM)	NP_001243098.1:n.326-18del
NR_045828.2:n.583-18del (APOM)