Canonical Allele Identifier: CA1397109296

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120674943G= , CM000665.2:g.120674943G=	GRCh38
NC_000003.11:g.120393790G= , CM000665.1:g.120393790G=	GRCh37
NC_000003.10:g.121876480G=	NCBI36
NG_011957.1:g.12539C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.134C= MANE Select	ENSP00000283871.5:p.Ser45=
ENST00000283871.9:c.134C=	ENSP00000283871.5:p.Ser45=
ENST00000466528.5:n.160C=
ENST00000476082.2:c.53+849C=	ENSP00000419560.2:n.53+849C=
ENST00000480862.1:n.292C=
ENST00000485313.5:n.242C=
ENST00000488183.5:n.392C=
NM_000187.3:c.134C=	NP_000178.2:p.Ser45=
XM_005247412.1:c.134C=	XP_005247469.1:p.Ser45=
XM_005247413.1:c.134C=	XP_005247470.1:p.Ser45=
XM_005247414.3:c.134C=	XP_005247471.1:p.Ser45=
XM_011512746.1:c.134C=	XP_011511048.1:p.Ser45=
XM_005247412.2:c.134C=	XP_005247469.1:p.Ser45=
XM_005247413.2:c.134C=	XP_005247470.1:p.Ser45=
XM_005247414.5:c.134C=	XP_005247471.1:p.Ser45=
XM_011512746.2:c.134C=	XP_011511048.1:p.Ser45=
XM_017006277.2:c.-290C=	XP_016861766.1:n.-290C=
NM_000187.4:c.134C= MANE Select	NP_000178.2:p.Ser45=