Canonical Allele Identifier: CA1397107334

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120670388T= , CM000665.2:g.120670388T=	GRCh38
NC_000003.11:g.120389235T= , CM000665.1:g.120389235T=	GRCh37
NC_000003.10:g.121871925T=	NCBI36
NG_011957.1:g.17094A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.282+39A= MANE Select	ENSP00000283871.5:n.282+39A=
ENST00000283871.9:c.282+39A=	ENSP00000283871.5:n.282+39A=
ENST00000466528.5:n.347A=
ENST00000476082.2:c.159+39A=	ENSP00000419560.2:n.159+39A=
ENST00000485313.5:n.390+39A=
ENST00000488183.5:n.540+39A=
NM_000187.3:c.282+39A=	NP_000178.2:n.282+39A=
XM_005247412.1:c.282+39A=	XP_005247469.1:n.282+39A=
XM_005247413.1:c.282+39A=	XP_005247470.1:n.282+39A=
XM_005247414.3:c.282+39A=	XP_005247471.1:n.282+39A=
XM_011512746.1:c.282+39A=	XP_011511048.1:n.282+39A=
XM_005247412.2:c.282+39A=	XP_005247469.1:n.282+39A=
XM_005247413.2:c.282+39A=	XP_005247470.1:n.282+39A=
XM_005247414.5:c.282+39A=	XP_005247471.1:n.282+39A=
XM_011512746.2:c.282+39A=	XP_011511048.1:n.282+39A=
XM_017006277.2:c.-142+39A=	XP_016861766.1:n.-142+39A=
NM_000187.4:c.282+39A= MANE Select	NP_000178.2:n.282+39A=