Canonical Allele Identifier: CA1619250148

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656060_31656062delinsCTG , CM000668.2:g.31656060_31656062delinsCTG	GRCh38
NC_000006.11:g.31623837_31623839delinsCTG , CM000668.1:g.31623837_31623839delinsCTG	GRCh37
NC_000006.10:g.31731816_31731818delinsCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.94_96delinsCTG (APOM) MANE Select	ENSP00000365081.3:p.Leu32=
ENST00000375916.3:c.94_96delinsCTG (APOM)	ENSP00000365081.3:p.Leu32=
ENST00000375918.6:c.-102-412_-102-410delinsCTG (APOM)	ENSP00000365083.2:n.-102-412_-102-410delinsCTG
ENST00000375920.8:c.-102-412_-102-410delinsCTG (APOM)	ENSP00000365085.4:n.-102-412_-102-410delinsCTG
NM_001256169.1:c.-102-412_-102-410delinsCTG (APOM)	NP_001243098.1:n.-102-412_-102-410delinsCTG
NM_019101.2:c.94_96delinsCTG (APOM)	NP_061974.2:p.Leu32=
NR_045828.1:n.143-412_143-410delinsCTG (APOM)
XM_006715150.2:c.-10_-8delinsCTG (APOM)	XP_006715213.1:n.-10_-8delinsCTG
XM_011514895.1:c.-14+4259_-14+4261delinsCAG (BAG6)	XP_011513197.1:n.-14+4259_-14+4261delinsCAG
XM_006715150.3:c.-10_-8delinsCTG (APOM)	XP_006715213.1:n.-10_-8delinsCTG
XM_017011279.2:c.-14+4259_-14+4261delinsCAG (BAG6)	XP_016866768.1:n.-14+4259_-14+4261delinsCAG
XM_024446545.1:c.-14+1702_-14+1704delinsCAG (BAG6)	XP_024302313.1:n.-14+1702_-14+1704delinsCAG
NM_019101.3:c.94_96delinsCTG (APOM) MANE Select	NP_061974.2:p.Leu32=
NM_001256169.2:c.-102-412_-102-410delinsCTG (APOM)	NP_001243098.1:n.-102-412_-102-410delinsCTG
NR_045828.2:n.149-412_149-410delinsCTG (APOM)