Canonical Allele Identifier: CA1619250980

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658103C= , CM000668.2:g.31658103C=	GRCh38
NC_000006.11:g.31625880C= , CM000668.1:g.31625880C=	GRCh37
NC_000006.10:g.31733859C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.*14C= (APOM) MANE Select	ENSP00000365081.3:n.*14C=
ENST00000375916.3:c.*14C= (APOM)	ENSP00000365081.3:n.*14C=
ENST00000375920.8:c.*14C= (APOM)	ENSP00000365085.4:n.*14C=
NM_001256169.1:c.*14C= (APOM)	NP_001243098.1:n.*14C=
NM_019101.2:c.*14C= (APOM)	NP_061974.2:n.*14C=
NR_045828.1:n.616C= (APOM)
XM_006715150.2:c.*14C= (APOM)	XP_006715213.1:n.*14C=
XM_011514895.1:c.-14+2218G= (BAG6)	XP_011513197.1:n.-14+2218G=
XM_006715150.3:c.*14C= (APOM)	XP_006715213.1:n.*14C=
XM_017011279.2:c.-14+2218G= (BAG6)	XP_016866768.1:n.-14+2218G=
NM_019101.3:c.*14C= (APOM) MANE Select	NP_061974.2:n.*14C=
NM_001256169.2:c.*14C= (APOM)	NP_001243098.1:n.*14C=
NR_045828.2:n.622C= (APOM)