Canonical Allele Identifier: CA1397107399

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120670531A= , CM000665.2:g.120670531A=	GRCh38
NC_000003.11:g.120389378A= , CM000665.1:g.120389378A=	GRCh37
NC_000003.10:g.121872068A=	NCBI36
NG_011957.1:g.16951T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.178T= MANE Select	ENSP00000283871.5:p.Trp60=
ENST00000283871.9:c.178T=	ENSP00000283871.5:p.Trp60=
ENST00000466528.5:n.204T=
ENST00000476082.2:c.55T=	ENSP00000419560.2:p.Trp19=
ENST00000485313.5:n.286T=
ENST00000488183.5:n.436T=
NM_000187.3:c.178T=	NP_000178.2:p.Trp60=
XM_005247412.1:c.178T=	XP_005247469.1:p.Trp60=
XM_005247413.1:c.178T=	XP_005247470.1:p.Trp60=
XM_005247414.3:c.178T=	XP_005247471.1:p.Trp60=
XM_011512746.1:c.178T=	XP_011511048.1:p.Trp60=
XM_005247412.2:c.178T=	XP_005247469.1:p.Trp60=
XM_005247413.2:c.178T=	XP_005247470.1:p.Trp60=
XM_005247414.5:c.178T=	XP_005247471.1:p.Trp60=
XM_011512746.2:c.178T=	XP_011511048.1:p.Trp60=
XM_017006277.2:c.-246T=	XP_016861766.1:n.-246T=
NM_000187.4:c.178T= MANE Select	NP_000178.2:p.Trp60=