Canonical Allele Identifier: CA1397109448

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120675251G= , CM000665.2:g.120675251G=	GRCh38
NC_000003.11:g.120394098G= , CM000665.1:g.120394098G=	GRCh37
NC_000003.10:g.121876788G=	NCBI36
NG_011957.1:g.12231C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.88-262C= MANE Select	ENSP00000283871.5:n.88-262C=
ENST00000283871.9:c.88-262C=	ENSP00000283871.5:n.88-262C=
ENST00000466528.5:n.114-262C=
ENST00000476082.2:c.53+541C=	ENSP00000419560.2:n.53+541C=
ENST00000480862.1:n.246-262C=
ENST00000485313.5:n.196-262C=
ENST00000488183.5:n.346-262C=
NM_000187.3:c.88-262C=	NP_000178.2:n.88-262C=
XM_005247412.1:c.88-262C=	XP_005247469.1:n.88-262C=
XM_005247413.1:c.88-262C=	XP_005247470.1:n.88-262C=
XM_005247414.3:c.88-262C=	XP_005247471.1:n.88-262C=
XM_011512746.1:c.88-262C=	XP_011511048.1:n.88-262C=
XM_005247412.2:c.88-262C=	XP_005247469.1:n.88-262C=
XM_005247413.2:c.88-262C=	XP_005247470.1:n.88-262C=
XM_005247414.5:c.88-262C=	XP_005247471.1:n.88-262C=
XM_011512746.2:c.88-262C=	XP_011511048.1:n.88-262C=
XM_017006277.2:c.-336-262C=	XP_016861766.1:n.-336-262C=
NM_000187.4:c.88-262C= MANE Select	NP_000178.2:n.88-262C=