Canonical Allele Identifier: CA1619250095

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655914T= , CM000668.2:g.31655914T=	GRCh38
NC_000006.11:g.31623691T= , CM000668.1:g.31623691T=	GRCh37
NC_000006.10:g.31731670T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.-53T= (APOM) MANE Select	ENSP00000365081.3:n.-53T=
ENST00000375916.3:c.-53T= (APOM)	ENSP00000365081.3:n.-53T=
ENST00000375918.6:c.-102-558T= (APOM)	ENSP00000365083.2:n.-102-558T=
ENST00000375920.8:c.-102-558T= (APOM)	ENSP00000365085.4:n.-102-558T=
NM_001256169.1:c.-102-558T= (APOM)	NP_001243098.1:n.-102-558T=
NM_019101.2:c.-53T= (APOM)	NP_061974.2:n.-53T=
NR_045828.1:n.143-558T= (APOM)
XM_006715150.2:c.-156T= (APOM)	XP_006715213.1:n.-156T=
XM_011514895.1:c.-13-4138A= (BAG6)	XP_011513197.1:n.-13-4138A=
XM_017011279.2:c.-13-4138A= (BAG6)	XP_016866768.1:n.-13-4138A=
XM_024446545.1:c.-14+1850A= (BAG6)	XP_024302313.1:n.-14+1850A=
NM_019101.3:c.-53T= (APOM) MANE Select	NP_061974.2:n.-53T=
NM_001256169.2:c.-102-558T= (APOM)	NP_001243098.1:n.-102-558T=
NR_045828.2:n.149-558T= (APOM)