Canonical Allele Identifier: CA2677982797

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31656188-GTGAGTGTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656189_31656196del , CM000668.2:g.31656189_31656196del	GRCh38
NC_000006.11:g.31623966_31623973del , CM000668.1:g.31623966_31623973del	GRCh37
NC_000006.10:g.31731945_31731952del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.114+109_114+116del (APOM) MANE Select	ENSP00000365081.3:n.114+109_114+116del
ENST00000375916.3:c.114+109_114+116del (APOM)	ENSP00000365081.3:n.114+109_114+116del
ENST00000375918.6:c.-102-283_-102-276del (APOM)	ENSP00000365083.2:n.-102-283_-102-276del
ENST00000375920.8:c.-102-283_-102-276del (APOM)	ENSP00000365085.4:n.-102-283_-102-276del
NM_001256169.1:c.-102-283_-102-276del (APOM)	NP_001243098.1:n.-102-283_-102-276del
NM_019101.2:c.114+109_114+116del (APOM)	NP_061974.2:n.114+109_114+116del
NR_045828.1:n.143-283_143-276del (APOM)
XM_006715150.2:c.11+109_11+116del (APOM)	XP_006715213.1:n.11+109_11+116del
XM_011514895.1:c.-14+4125_-14+4132del (BAG6)	XP_011513197.1:n.-14+4125_-14+4132del
XM_006715150.3:c.11+109_11+116del (APOM)	XP_006715213.1:n.11+109_11+116del
XM_017011279.2:c.-14+4125_-14+4132del (BAG6)	XP_016866768.1:n.-14+4125_-14+4132del
XM_024446545.1:c.-14+1568_-14+1575del (BAG6)	XP_024302313.1:n.-14+1568_-14+1575del
NM_019101.3:c.114+109_114+116del (APOM) MANE Select	NP_061974.2:n.114+109_114+116del
NM_001256169.2:c.-102-283_-102-276del (APOM)	NP_001243098.1:n.-102-283_-102-276del
NR_045828.2:n.149-283_149-276del (APOM)