Canonical Allele Identifier: CA2677982589

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31656021-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656023dup , CM000668.2:g.31656023dup	GRCh38
NC_000006.11:g.31623800dup , CM000668.1:g.31623800dup	GRCh37
NC_000006.10:g.31731779dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.57dup (APOM) MANE Select	ENSP00000365081.3:p.Ile20HisfsTer6
ENST00000375916.3:c.57dup (APOM)	ENSP00000365081.3:p.Ile20HisfsTer6
ENST00000375918.6:c.-102-449dup (APOM)	ENSP00000365083.2:n.-102-449dup
ENST00000375920.8:c.-102-449dup (APOM)	ENSP00000365085.4:n.-102-449dup
NM_001256169.1:c.-102-449dup (APOM)	NP_001243098.1:n.-102-449dup
NM_019101.2:c.57dup (APOM)	NP_061974.2:p.Ile20HisfsTer6
NR_045828.1:n.143-449dup (APOM)
XM_006715150.2:c.-47dup (APOM)	XP_006715213.1:n.-47dup
XM_011514895.1:c.-13-4246dup (BAG6)	XP_011513197.1:n.-13-4246dup
XM_006715150.3:c.-47dup (APOM)	XP_006715213.1:n.-47dup
XM_017011279.2:c.-13-4246dup (BAG6)	XP_016866768.1:n.-13-4246dup
XM_024446545.1:c.-14+1742dup (BAG6)	XP_024302313.1:n.-14+1742dup
NM_019101.3:c.57dup (APOM) MANE Select	NP_061974.2:p.Ile20HisfsTer6
NM_001256169.2:c.-102-449dup (APOM)	NP_001243098.1:n.-102-449dup
NR_045828.2:n.149-449dup (APOM)