Canonical Allele Identifier: CA2677983041

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31656444-TCTTTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656447_31656452del , CM000668.2:g.31656447_31656452del	GRCh38
NC_000006.11:g.31624224_31624229del , CM000668.1:g.31624224_31624229del	GRCh37
NC_000006.10:g.31732203_31732208del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.115-25_115-20del (APOM) MANE Select	ENSP00000365081.3:n.115-25_115-20del
ENST00000375916.3:c.115-25_115-20del (APOM)	ENSP00000365081.3:n.115-25_115-20del
ENST00000375918.6:c.-102-25_-102-20del (APOM)	ENSP00000365083.2:n.-102-25_-102-20del
ENST00000375920.8:c.-102-25_-102-20del (APOM)	ENSP00000365085.4:n.-102-25_-102-20del
NM_001256169.1:c.-102-25_-102-20del (APOM)	NP_001243098.1:n.-102-25_-102-20del
NM_019101.2:c.115-25_115-20del (APOM)	NP_061974.2:n.115-25_115-20del
NR_045828.1:n.143-25_143-20del (APOM)
XM_006715150.2:c.12-25_12-20del (APOM)	XP_006715213.1:n.12-25_12-20del
XM_011514895.1:c.-14+3871_-14+3876del (BAG6)	XP_011513197.1:n.-14+3871_-14+3876del
XM_006715150.3:c.12-25_12-20del (APOM)	XP_006715213.1:n.12-25_12-20del
XM_017011279.2:c.-14+3871_-14+3876del (BAG6)	XP_016866768.1:n.-14+3871_-14+3876del
XM_024446545.1:c.-14+1314_-14+1319del (BAG6)	XP_024302313.1:n.-14+1314_-14+1319del
NM_019101.3:c.115-25_115-20del (APOM) MANE Select	NP_061974.2:n.115-25_115-20del
NM_001256169.2:c.-102-25_-102-20del (APOM)	NP_001243098.1:n.-102-25_-102-20del
NR_045828.2:n.149-25_149-20del (APOM)