Canonical Allele Identifier: CA1619250391

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656665C= , CM000668.2:g.31656665C=	GRCh38
NC_000006.11:g.31624442C= , CM000668.1:g.31624442C=	GRCh37
NC_000006.10:g.31732421C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.269+39C= (APOM) MANE Select	ENSP00000365081.3:n.269+39C=
ENST00000375916.3:c.269+39C= (APOM)	ENSP00000365081.3:n.269+39C=
ENST00000375918.6:c.53+39C= (APOM)	ENSP00000365083.2:n.53+39C=
ENST00000375920.8:c.53+39C= (APOM)	ENSP00000365085.4:n.53+39C=
NM_001256169.1:c.53+39C= (APOM)	NP_001243098.1:n.53+39C=
NM_019101.2:c.269+39C= (APOM)	NP_061974.2:n.269+39C=
NR_045828.1:n.304+32C= (APOM)
XM_006715150.2:c.173+32C= (APOM)	XP_006715213.1:n.173+32C=
XM_011514895.1:c.-14+3656G= (BAG6)	XP_011513197.1:n.-14+3656G=
XM_006715150.3:c.173+32C= (APOM)	XP_006715213.1:n.173+32C=
XM_017011279.2:c.-14+3656G= (BAG6)	XP_016866768.1:n.-14+3656G=
XM_024446545.1:c.-14+1099G= (BAG6)	XP_024302313.1:n.-14+1099G=
NM_019101.3:c.269+39C= (APOM) MANE Select	NP_061974.2:n.269+39C=
NM_001256169.2:c.53+39C= (APOM)	NP_001243098.1:n.53+39C=
NR_045828.2:n.310+32C= (APOM)