Canonical Allele Identifier: CA1397099257

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120652400T= , CM000665.2:g.120652400T=	GRCh38
NC_000003.11:g.120371247T= , CM000665.1:g.120371247T=	GRCh37
NC_000003.10:g.121853937T=	NCBI36
NG_011957.1:g.35082A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.342+192A= MANE Select	ENSP00000283871.5:n.342+192A=
ENST00000283871.9:c.342+192A=	ENSP00000283871.5:n.342+192A=
ENST00000476082.2:c.219+192A=	ENSP00000419560.2:n.219+192A=
ENST00000485313.5:n.450+192A=
NM_000187.3:c.342+192A=	NP_000178.2:n.342+192A=
XM_005247412.1:c.342+192A=	XP_005247469.1:n.342+192A=
XM_005247413.1:c.342+192A=	XP_005247470.1:n.342+192A=
XM_005247414.3:c.342+192A=	XP_005247471.1:n.342+192A=
XM_011512746.1:c.342+192A=	XP_011511048.1:n.342+192A=
XM_005247412.2:c.342+192A=	XP_005247469.1:n.342+192A=
XM_005247413.2:c.342+192A=	XP_005247470.1:n.342+192A=
XM_005247414.5:c.342+192A=	XP_005247471.1:n.342+192A=
XM_011512746.2:c.342+192A=	XP_011511048.1:n.342+192A=
XM_017006277.2:c.-82+192A=	XP_016861766.1:n.-82+192A=
NM_000187.4:c.342+192A= MANE Select	NP_000178.2:n.342+192A=