Canonical Allele Identifier: CA2677984159

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31658050-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658056dup , CM000668.2:g.31658056dup	GRCh38
NC_000006.11:g.31625833dup , CM000668.1:g.31625833dup	GRCh37
NC_000006.10:g.31733812dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.542-8dup (APOM) MANE Select	ENSP00000365081.3:n.542-8dup
ENST00000375916.3:c.542-8dup (APOM)	ENSP00000365081.3:n.542-8dup
ENST00000375918.6:c.*268dup (APOM)	ENSP00000365083.2:n.*268dup
ENST00000375920.8:c.326-8dup (APOM)	ENSP00000365085.4:n.326-8dup
NM_001256169.1:c.326-8dup (APOM)	NP_001243098.1:n.326-8dup
NM_019101.2:c.542-8dup (APOM)	NP_061974.2:n.542-8dup
NR_045828.1:n.577-8dup (APOM)
XM_006715150.2:c.446-8dup (APOM)	XP_006715213.1:n.446-8dup
XM_011514895.1:c.-14+2270dup (BAG6)	XP_011513197.1:n.-14+2270dup
XM_006715150.3:c.446-8dup (APOM)	XP_006715213.1:n.446-8dup
XM_017011279.2:c.-14+2270dup (BAG6)	XP_016866768.1:n.-14+2270dup
NM_019101.3:c.542-8dup (APOM) MANE Select	NP_061974.2:n.542-8dup
NM_001256169.2:c.326-8dup (APOM)	NP_001243098.1:n.326-8dup
NR_045828.2:n.583-8dup (APOM)