Canonical Allele Identifier: CA2770516640

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656186dup , CM000668.2:g.31656186dup	GRCh38
NC_000006.11:g.31623963dup , CM000668.1:g.31623963dup	GRCh37
NC_000006.10:g.31731942dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.114+106dup (APOM) MANE Select	ENSP00000365081.3:n.114+106dup
ENST00000375916.3:c.114+106dup (APOM)	ENSP00000365081.3:n.114+106dup
ENST00000375918.6:c.-102-286dup (APOM)	ENSP00000365083.2:n.-102-286dup
ENST00000375920.8:c.-102-286dup (APOM)	ENSP00000365085.4:n.-102-286dup
NM_001256169.1:c.-102-286dup (APOM)	NP_001243098.1:n.-102-286dup
NM_019101.2:c.114+106dup (APOM)	NP_061974.2:n.114+106dup
NR_045828.1:n.143-286dup (APOM)
XM_006715150.2:c.11+106dup (APOM)	XP_006715213.1:n.11+106dup
XM_011514895.1:c.-14+4139dup (BAG6)	XP_011513197.1:n.-14+4139dup
XM_006715150.3:c.11+106dup (APOM)	XP_006715213.1:n.11+106dup
XM_017011279.2:c.-14+4139dup (BAG6)	XP_016866768.1:n.-14+4139dup
XM_024446545.1:c.-14+1582dup (BAG6)	XP_024302313.1:n.-14+1582dup
NM_019101.3:c.114+106dup (APOM) MANE Select	NP_061974.2:n.114+106dup
NM_001256169.2:c.-102-286dup (APOM)	NP_001243098.1:n.-102-286dup
NR_045828.2:n.149-286dup (APOM)