Canonical Allele Identifier: CA1397093026

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120638364A= , CM000665.2:g.120638364A=	GRCh38
NC_000003.11:g.120357211A= , CM000665.1:g.120357211A=	GRCh37
NC_000003.10:g.121839901A=	NCBI36
NG_011957.1:g.49118T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.1006+91T= MANE Select	ENSP00000283871.5:n.1006+91T=
ENST00000283871.9:c.1006+91T=	ENSP00000283871.5:n.1006+91T=
ENST00000470321.1:n.346+91T=
ENST00000475447.2:c.307+3225T=
ENST00000492108.5:c.285+3225T=	ENSP00000419838.1:n.285+3225T=
ENST00000494453.1:c.426+91T=
NM_000187.3:c.1006+91T=	NP_000178.2:n.1006+91T=
XM_005247412.1:c.781+91T=	XP_005247469.1:n.781+91T=
XM_005247413.1:c.1006+91T=	XP_005247470.1:n.1006+91T=
XM_011512746.1:c.879+3225T=	XP_011511048.1:n.879+3225T=
XM_005247412.2:c.781+91T=	XP_005247469.1:n.781+91T=
XM_005247413.2:c.1006+91T=	XP_005247470.1:n.1006+91T=
XM_011512746.2:c.879+3225T=	XP_011511048.1:n.879+3225T=
XM_017006277.2:c.583+91T=	XP_016861766.1:n.583+91T=
NM_000187.4:c.1006+91T= MANE Select	NP_000178.2:n.1006+91T=