Canonical Allele Identifier: CA1619250827

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657691C= , CM000668.2:g.31657691C=	GRCh38
NC_000006.11:g.31625468C= , CM000668.1:g.31625468C=	GRCh37
NC_000006.10:g.31733447C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.509C= (APOM) MANE Select	ENSP00000365081.3:p.Ser170=
ENST00000375916.3:c.509C= (APOM)	ENSP00000365081.3:p.Ser170=
ENST00000375918.6:c.293C= (APOM)	ENSP00000365083.2:p.Ser98=
ENST00000375920.8:c.293C= (APOM)	ENSP00000365085.4:p.Ser98=
NM_001256169.1:c.293C= (APOM)	NP_001243098.1:p.Ser98=
NM_019101.2:c.509C= (APOM)	NP_061974.2:p.Ser170=
NR_045828.1:n.544C= (APOM)
XM_006715150.2:c.413C= (APOM)	XP_006715213.1:p.Ser138=
XM_011514895.1:c.-14+2630G= (BAG6)	XP_011513197.1:n.-14+2630G=
XM_006715150.3:c.413C= (APOM)	XP_006715213.1:p.Ser138=
XM_017011279.2:c.-14+2630G= (BAG6)	XP_016866768.1:n.-14+2630G=
XM_024446545.1:c.-14+73G= (BAG6)	XP_024302313.1:n.-14+73G=
NM_019101.3:c.509C= (APOM) MANE Select	NP_061974.2:p.Ser170=
NM_001256169.2:c.293C= (APOM)	NP_001243098.1:p.Ser98=
NR_045828.2:n.550C= (APOM)