Canonical Allele Identifier: CA1619250062

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655831A= , CM000668.2:g.31655831A=	GRCh38
NC_000006.11:g.31623608A= , CM000668.1:g.31623608A=	GRCh37
NC_000006.10:g.31731587A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.3:c.-136A= (APOM)	ENSP00000365081.3:n.-136A=
ENST00000375918.6:c.-102-641A= (APOM)	ENSP00000365083.2:n.-102-641A=
ENST00000375920.8:c.-102-641A= (APOM)	ENSP00000365085.4:n.-102-641A=
NM_001256169.1:c.-102-641A= (APOM)	NP_001243098.1:n.-102-641A=
NR_045828.1:n.143-641A= (APOM)
XM_006715150.2:c.-239A= (APOM)	XP_006715213.1:n.-239A=
XM_011514895.1:c.-13-4055T= (BAG6)	XP_011513197.1:n.-13-4055T=
XM_017011279.2:c.-13-4055T= (BAG6)	XP_016866768.1:n.-13-4055T=
XM_024446545.1:c.-14+1933T= (BAG6)	XP_024302313.1:n.-14+1933T=
NM_001256169.2:c.-102-641A= (APOM)	NP_001243098.1:n.-102-641A=
NR_045828.2:n.149-641A= (APOM)