Canonical Allele Identifier: CA1397096903

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120647041C= , CM000665.2:g.120647041C=	GRCh38
NC_000003.11:g.120365888C= , CM000665.1:g.120365888C=	GRCh37
NC_000003.10:g.121848578C=	NCBI36
NG_011957.1:g.40441G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000187.4:c.481G= MANE Select	NP_000178.2:p.Gly161=
ENST00000283871.10:c.481G= MANE Select	ENSP00000283871.5:p.Gly161=
NM_000187.3:c.481G=	NP_000178.2:p.Gly161=
ENST00000283871.9:c.481G=	ENSP00000283871.5:p.Gly161=
ENST00000475447.2:c.12G=
ENST00000476082.2:c.358G=	ENSP00000419560.2:p.Gly120=
ENST00000492108.5:c.112G=	ENSP00000419838.1:p.Gly38=
XM_005247412.1:c.481G=	XP_005247469.1:p.Gly161=
XM_005247412.2:c.481G=	XP_005247469.1:p.Gly161=
XM_005247413.1:c.481G=	XP_005247470.1:p.Gly161=
XM_005247413.2:c.481G=	XP_005247470.1:p.Gly161=
XM_005247414.3:c.481G=	XP_005247471.1:p.Gly161=
XM_005247414.5:c.481G=	XP_005247471.1:p.Gly161=
XM_011512746.1:c.481G=	XP_011511048.1:p.Gly161=
XM_011512746.2:c.481G=	XP_011511048.1:p.Gly161=
XM_017006277.2:c.58G=	XP_016861766.1:p.Gly20=