Canonical Allele Identifier: CA2667173267

Gene: HGD

Linked Data

• gnomAD v4: 3-120675693-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120675693A>T , CM000665.2:g.120675693A>T	GRCh38
NC_000003.11:g.120394540A>T , CM000665.1:g.120394540A>T	GRCh37
NC_000003.10:g.121877230A>T	NCBI36
NG_011957.1:g.11789T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.87+99T>A MANE Select	ENSP00000283871.5:n.87+99T>A
ENST00000283871.9:c.87+99T>A	ENSP00000283871.5:n.87+99T>A
ENST00000466528.5:n.113+99T>A
ENST00000476082.2:c.53+99T>A	ENSP00000419560.2:n.53+99T>A
ENST00000480862.1:n.245+99T>A
ENST00000485313.5:n.195+99T>A
ENST00000488183.5:n.345+99T>A
NM_000187.3:c.87+99T>A	NP_000178.2:n.87+99T>A
XM_005247412.1:c.87+99T>A	XP_005247469.1:n.87+99T>A
XM_005247413.1:c.87+99T>A	XP_005247470.1:n.87+99T>A
XM_005247414.3:c.87+99T>A	XP_005247471.1:n.87+99T>A
XM_011512746.1:c.87+99T>A	XP_011511048.1:n.87+99T>A
XM_005247412.2:c.87+99T>A	XP_005247469.1:n.87+99T>A
XM_005247413.2:c.87+99T>A	XP_005247470.1:n.87+99T>A
XM_005247414.5:c.87+99T>A	XP_005247471.1:n.87+99T>A
XM_011512746.2:c.87+99T>A	XP_011511048.1:n.87+99T>A
XM_017006277.2:c.-337+99T>A	XP_016861766.1:n.-337+99T>A
NM_000187.4:c.87+99T>A MANE Select	NP_000178.2:n.87+99T>A