Canonical Allele Identifier: CA1619250998

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658136T= , CM000668.2:g.31658136T=	GRCh38
NC_000006.11:g.31625913T= , CM000668.1:g.31625913T=	GRCh37
NC_000006.10:g.31733892T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.*47T= (APOM) MANE Select	ENSP00000365081.3:n.*47T=
ENST00000375916.3:c.*47T= (APOM)	ENSP00000365081.3:n.*47T=
ENST00000375920.8:c.*47T= (APOM)	ENSP00000365085.4:n.*47T=
NM_001256169.1:c.*47T= (APOM)	NP_001243098.1:n.*47T=
NM_019101.2:c.*47T= (APOM)	NP_061974.2:n.*47T=
NR_045828.1:n.649T= (APOM)
XM_006715150.2:c.*47T= (APOM)	XP_006715213.1:n.*47T=
XM_011514895.1:c.-14+2185A= (BAG6)	XP_011513197.1:n.-14+2185A=
XM_006715150.3:c.*47T= (APOM)	XP_006715213.1:n.*47T=
XM_017011279.2:c.-14+2185A= (BAG6)	XP_016866768.1:n.-14+2185A=
NM_019101.3:c.*47T= (APOM) MANE Select	NP_061974.2:n.*47T=
NM_001256169.2:c.*47T= (APOM)	NP_001243098.1:n.*47T=
NR_045828.2:n.655T= (APOM)