Canonical Allele Identifier: CA1397093081

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120638488C= , CM000665.2:g.120638488C=	GRCh38
NC_000003.11:g.120357335C= , CM000665.1:g.120357335C=	GRCh37
NC_000003.10:g.121840025C=	NCBI36
NG_011957.1:g.48994G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.973G= MANE Select	ENSP00000283871.5:p.Ala325=
ENST00000283871.9:c.973G=	ENSP00000283871.5:p.Ala325=
ENST00000470321.1:n.313G=
ENST00000475447.2:c.307+3101G=
ENST00000492108.5:c.285+3101G=	ENSP00000419838.1:n.285+3101G=
ENST00000494453.1:c.393G=
NM_000187.3:c.973G=	NP_000178.2:p.Ala325=
XM_005247412.1:c.748G=	XP_005247469.1:p.Ala250=
XM_005247413.1:c.973G=	XP_005247470.1:p.Ala325=
XM_011512746.1:c.879+3101G=	XP_011511048.1:n.879+3101G=
XM_005247412.2:c.748G=	XP_005247469.1:p.Ala250=
XM_005247413.2:c.973G=	XP_005247470.1:p.Ala325=
XM_011512746.2:c.879+3101G=	XP_011511048.1:n.879+3101G=
XM_017006277.2:c.550G=	XP_016861766.1:p.Ala184=
NM_000187.4:c.973G= MANE Select	NP_000178.2:p.Ala325=