Canonical Allele Identifier: CA1619250729

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657451C= , CM000668.2:g.31657451C=	GRCh38
NC_000006.11:g.31625228C= , CM000668.1:g.31625228C=	GRCh37
NC_000006.10:g.31733207C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.415C= (APOM) MANE Select	ENSP00000365081.3:p.Gln139=
ENST00000375916.3:c.415C= (APOM)	ENSP00000365081.3:p.Gln139=
ENST00000375918.6:c.199C= (APOM)	ENSP00000365083.2:p.Gln67=
ENST00000375920.8:c.199C= (APOM)	ENSP00000365085.4:p.Gln67=
NM_001256169.1:c.199C= (APOM)	NP_001243098.1:p.Gln67=
NM_019101.2:c.415C= (APOM)	NP_061974.2:p.Gln139=
NR_045828.1:n.450C= (APOM)
XM_006715150.2:c.319C= (APOM)	XP_006715213.1:p.Gln107=
XM_011514895.1:c.-14+2870G= (BAG6)	XP_011513197.1:n.-14+2870G=
XM_006715150.3:c.319C= (APOM)	XP_006715213.1:p.Gln107=
XM_017011279.2:c.-14+2870G= (BAG6)	XP_016866768.1:n.-14+2870G=
XM_024446545.1:c.-14+313G= (BAG6)	XP_024302313.1:n.-14+313G=
NM_019101.3:c.415C= (APOM) MANE Select	NP_061974.2:p.Gln139=
NM_001256169.2:c.199C= (APOM)	NP_001243098.1:p.Gln67=
NR_045828.2:n.456C= (APOM)