Canonical Allele Identifier: CA1397109734

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120675874C= , CM000665.2:g.120675874C=	GRCh38
NC_000003.11:g.120394721C= , CM000665.1:g.120394721C=	GRCh37
NC_000003.10:g.121877411C=	NCBI36
NG_011957.1:g.11608G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.16-11G= MANE Select	ENSP00000283871.5:n.16-11G=
ENST00000283871.9:c.16-11G=	ENSP00000283871.5:n.16-11G=
ENST00000466528.5:n.42-11G=
ENST00000476082.2:c.-19-11G=	ENSP00000419560.2:n.-19-11G=
ENST00000480862.1:n.174-11G=
ENST00000485313.5:n.124-11G=
ENST00000488183.5:n.274-11G=
NM_000187.3:c.16-11G=	NP_000178.2:n.16-11G=
XM_005247412.1:c.16-11G=	XP_005247469.1:n.16-11G=
XM_005247413.1:c.16-11G=	XP_005247470.1:n.16-11G=
XM_005247414.3:c.16-11G=	XP_005247471.1:n.16-11G=
XM_011512746.1:c.16-11G=	XP_011511048.1:n.16-11G=
XM_005247412.2:c.16-11G=	XP_005247469.1:n.16-11G=
XM_005247413.2:c.16-11G=	XP_005247470.1:n.16-11G=
XM_005247414.5:c.16-11G=	XP_005247471.1:n.16-11G=
XM_011512746.2:c.16-11G=	XP_011511048.1:n.16-11G=
XM_017006277.2:c.-408-11G=	XP_016861766.1:n.-408-11G=
NM_000187.4:c.16-11G= MANE Select	NP_000178.2:n.16-11G=