Canonical Allele Identifier: CA1619250732

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657462G= , CM000668.2:g.31657462G=	GRCh38
NC_000006.11:g.31625239G= , CM000668.1:g.31625239G=	GRCh37
NC_000006.10:g.31733218G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.426G= (APOM) MANE Select	ENSP00000365081.3:p.Gln142=
ENST00000375916.3:c.426G= (APOM)	ENSP00000365081.3:p.Gln142=
ENST00000375918.6:c.210G= (APOM)	ENSP00000365083.2:p.Gln70=
ENST00000375920.8:c.210G= (APOM)	ENSP00000365085.4:p.Gln70=
NM_001256169.1:c.210G= (APOM)	NP_001243098.1:p.Gln70=
NM_019101.2:c.426G= (APOM)	NP_061974.2:p.Gln142=
NR_045828.1:n.461G= (APOM)
XM_006715150.2:c.330G= (APOM)	XP_006715213.1:p.Gln110=
XM_011514895.1:c.-14+2859C= (BAG6)	XP_011513197.1:n.-14+2859C=
XM_006715150.3:c.330G= (APOM)	XP_006715213.1:p.Gln110=
XM_017011279.2:c.-14+2859C= (BAG6)	XP_016866768.1:n.-14+2859C=
XM_024446545.1:c.-14+302C= (BAG6)	XP_024302313.1:n.-14+302C=
NM_019101.3:c.426G= (APOM) MANE Select	NP_061974.2:p.Gln142=
NM_001256169.2:c.210G= (APOM)	NP_001243098.1:p.Gln70=
NR_045828.2:n.467G= (APOM)