Canonical Allele Identifier: CA1619250649

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657283G= , CM000668.2:g.31657283G=	GRCh38
NC_000006.11:g.31625060G= , CM000668.1:g.31625060G=	GRCh37
NC_000006.10:g.31733039G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.328G= (APOM) MANE Select	ENSP00000365081.3:p.Asp110=
ENST00000375916.3:c.328G= (APOM)	ENSP00000365081.3:p.Asp110=
ENST00000375918.6:c.112G= (APOM)	ENSP00000365083.2:p.Asp38=
ENST00000375920.8:c.112G= (APOM)	ENSP00000365085.4:p.Asp38=
NM_001256169.1:c.112G= (APOM)	NP_001243098.1:p.Asp38=
NM_019101.2:c.328G= (APOM)	NP_061974.2:p.Asp110=
NR_045828.1:n.363G= (APOM)
XM_006715150.2:c.232G= (APOM)	XP_006715213.1:p.Asp78=
XM_011514895.1:c.-14+3038C= (BAG6)	XP_011513197.1:n.-14+3038C=
XM_006715150.3:c.232G= (APOM)	XP_006715213.1:p.Asp78=
XM_017011279.2:c.-14+3038C= (BAG6)	XP_016866768.1:n.-14+3038C=
XM_024446545.1:c.-14+481C= (BAG6)	XP_024302313.1:n.-14+481C=
NM_019101.3:c.328G= (APOM) MANE Select	NP_061974.2:p.Asp110=
NM_001256169.2:c.112G= (APOM)	NP_001243098.1:p.Asp38=
NR_045828.2:n.369G= (APOM)