Canonical Allele Identifier: CA2322262028

Gene: ANGPTL6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10102478G= , CM000681.2:g.10102478G=	GRCh38
NC_000019.9:g.10213154G= , CM000681.1:g.10213154G=	GRCh37
NC_000019.8:g.10074154G=	NCBI36
NG_051640.1:g.1256G=

Transcript Alleles

HGVS	Amino-acid Change
NM_031917.3:c.-11+90C= MANE Select	NP_114123.2:n.-11+90C=
ENST00000253109.5:c.-11+90C= MANE Select	ENSP00000253109.3:n.-11+90C=
NM_001321411.1:c.-11+74C=	NP_001308340.1:n.-11+74C=
NM_001321411.2:c.-11+74C=	NP_001308340.1:n.-11+74C=
NM_001387347.1:c.-11+90C=	NP_001374276.1:n.-11+90C=
NM_001387348.1:c.-11+90C=	NP_001374277.1:n.-11+90C=
NM_031917.2:c.-11+90C=	NP_114123.2:n.-11+90C=
ENST00000253109.4:c.-11+90C=	ENSP00000253109.3:n.-11+90C=
ENST00000592641.5:c.-11+74C=	ENSP00000467930.1:n.-11+74C=
XM_005260091.2:c.233+74C=	XP_005260148.1:n.233+74C=
XM_005260091.4:c.233+74C=	XP_005260148.1:n.233+74C=
XM_011528347.1:c.-11+90C=	XP_011526649.1:n.-11+90C=
XM_011528347.3:c.-11+90C=	XP_011526649.1:n.-11+90C=
XM_011528348.1:c.191+74C=	XP_011526650.1:n.191+74C=
XM_011528348.3:c.191+74C=	XP_011526650.1:n.191+74C=
XM_011528349.1:c.191+74C=	XP_011526651.1:n.191+74C=
XM_011528349.3:c.191+74C=	XP_011526651.1:n.191+74C=
XM_011528350.1:c.-11+90C=	XP_011526652.1:n.-11+90C=
XM_011528350.3:c.-11+90C=	XP_011526652.1:n.-11+90C=
XM_017027347.2:c.-11+90C=	XP_016882836.1:n.-11+90C=
XR_002958369.1:n.424+90C=