Canonical Allele Identifier: CA1397094569

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120641751T= , CM000665.2:g.120641751T=	GRCh38
NC_000003.11:g.120360598T= , CM000665.1:g.120360598T=	GRCh37
NC_000003.10:g.121843288T=	NCBI36
NG_011957.1:g.45731A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.775-58A= MANE Select	ENSP00000283871.5:n.775-58A=
ENST00000283871.9:c.775-58A=	ENSP00000283871.5:n.775-58A=
ENST00000470321.1:n.57A=
ENST00000475447.2:c.203-58A=
ENST00000492108.5:c.181-58A=	ENSP00000419838.1:n.181-58A=
ENST00000494453.1:c.195-58A=
NM_000187.3:c.775-58A=	NP_000178.2:n.775-58A=
XM_005247412.1:c.550-58A=	XP_005247469.1:n.550-58A=
XM_005247413.1:c.775-58A=	XP_005247470.1:n.775-58A=
XM_011512746.1:c.775-58A=	XP_011511048.1:n.775-58A=
XM_005247412.2:c.550-58A=	XP_005247469.1:n.550-58A=
XM_005247413.2:c.775-58A=	XP_005247470.1:n.775-58A=
XM_011512746.2:c.775-58A=	XP_011511048.1:n.775-58A=
XM_017006277.2:c.352-58A=	XP_016861766.1:n.352-58A=
NM_000187.4:c.775-58A= MANE Select	NP_000178.2:n.775-58A=