Canonical Allele Identifier: CA1397096586

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120646365C= , CM000665.2:g.120646365C=	GRCh38
NC_000003.11:g.120365212C= , CM000665.1:g.120365212C=	GRCh37
NC_000003.10:g.121847902C=	NCBI36
NG_011957.1:g.41117G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.551G= MANE Select	ENSP00000283871.5:p.Arg184=
ENST00000283871.9:c.551G=	ENSP00000283871.5:p.Arg184=
ENST00000475447.2:c.82G=
ENST00000492108.5:c.180+608G=	ENSP00000419838.1:n.180+608G=
NM_000187.3:c.551G=	NP_000178.2:p.Arg184=
XM_005247412.1:c.549+608G=	XP_005247469.1:n.549+608G=
XM_005247413.1:c.551G=	XP_005247470.1:p.Arg184=
XM_005247414.3:c.551G=	XP_005247471.1:p.Arg184=
XM_011512746.1:c.551G=	XP_011511048.1:p.Arg184=
XM_005247412.2:c.549+608G=	XP_005247469.1:n.549+608G=
XM_005247413.2:c.551G=	XP_005247470.1:p.Arg184=
XM_005247414.5:c.551G=	XP_005247471.1:p.Arg184=
XM_011512746.2:c.551G=	XP_011511048.1:p.Arg184=
XM_017006277.2:c.128G=	XP_016861766.1:p.Arg43=
NM_000187.4:c.551G= MANE Select	NP_000178.2:p.Arg184=