Canonical Allele Identifier: CA2677982801

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31656191-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656194_31656195del , CM000668.2:g.31656194_31656195del	GRCh38
NC_000006.11:g.31623971_31623972del , CM000668.1:g.31623971_31623972del	GRCh37
NC_000006.10:g.31731950_31731951del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.114+114_114+115del (APOM) MANE Select	ENSP00000365081.3:n.114+114_114+115del
ENST00000375916.3:c.114+114_114+115del (APOM)	ENSP00000365081.3:n.114+114_114+115del
ENST00000375918.6:c.-102-278_-102-277del (APOM)	ENSP00000365083.2:n.-102-278_-102-277del
ENST00000375920.8:c.-102-278_-102-277del (APOM)	ENSP00000365085.4:n.-102-278_-102-277del
NM_001256169.1:c.-102-278_-102-277del (APOM)	NP_001243098.1:n.-102-278_-102-277del
NM_019101.2:c.114+114_114+115del (APOM)	NP_061974.2:n.114+114_114+115del
NR_045828.1:n.143-278_143-277del (APOM)
XM_006715150.2:c.11+114_11+115del (APOM)	XP_006715213.1:n.11+114_11+115del
XM_011514895.1:c.-14+4128_-14+4129del (BAG6)	XP_011513197.1:n.-14+4128_-14+4129del
XM_006715150.3:c.11+114_11+115del (APOM)	XP_006715213.1:n.11+114_11+115del
XM_017011279.2:c.-14+4128_-14+4129del (BAG6)	XP_016866768.1:n.-14+4128_-14+4129del
XM_024446545.1:c.-14+1571_-14+1572del (BAG6)	XP_024302313.1:n.-14+1571_-14+1572del
NM_019101.3:c.114+114_114+115del (APOM) MANE Select	NP_061974.2:n.114+114_114+115del
NM_001256169.2:c.-102-278_-102-277del (APOM)	NP_001243098.1:n.-102-278_-102-277del
NR_045828.2:n.149-278_149-277del (APOM)