Canonical Allele Identifier: CA1619250798

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657617C= , CM000668.2:g.31657617C=	GRCh38
NC_000006.11:g.31625394C= , CM000668.1:g.31625394C=	GRCh37
NC_000006.10:g.31733373C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.443-8C= (APOM) MANE Select	ENSP00000365081.3:n.443-8C=
ENST00000375916.3:c.443-8C= (APOM)	ENSP00000365081.3:n.443-8C=
ENST00000375918.6:c.227-8C= (APOM)	ENSP00000365083.2:n.227-8C=
ENST00000375920.8:c.227-8C= (APOM)	ENSP00000365085.4:n.227-8C=
NM_001256169.1:c.227-8C= (APOM)	NP_001243098.1:n.227-8C=
NM_019101.2:c.443-8C= (APOM)	NP_061974.2:n.443-8C=
NR_045828.1:n.478-8C= (APOM)
XM_006715150.2:c.347-8C= (APOM)	XP_006715213.1:n.347-8C=
XM_011514895.1:c.-14+2704G= (BAG6)	XP_011513197.1:n.-14+2704G=
XM_006715150.3:c.347-8C= (APOM)	XP_006715213.1:n.347-8C=
XM_017011279.2:c.-14+2704G= (BAG6)	XP_016866768.1:n.-14+2704G=
XM_024446545.1:c.-14+147G= (BAG6)	XP_024302313.1:n.-14+147G=
NM_019101.3:c.443-8C= (APOM) MANE Select	NP_061974.2:n.443-8C=
NM_001256169.2:c.227-8C= (APOM)	NP_001243098.1:n.227-8C=
NR_045828.2:n.484-8C= (APOM)