Canonical Allele Identifier: CA2667171652

Gene: HGD

Linked Data

• gnomAD v4: 3-120646166-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120646166G>T , CM000665.2:g.120646166G>T	GRCh38
NC_000003.11:g.120365013G>T , CM000665.1:g.120365013G>T	GRCh37
NC_000003.10:g.121847703G>T	NCBI36
NG_011957.1:g.41316C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.649+101C>A MANE Select	ENSP00000283871.5:n.649+101C>A
ENST00000283871.9:c.649+101C>A	ENSP00000283871.5:n.649+101C>A
ENST00000475447.2:c.180+101C>A
ENST00000492108.5:c.180+807C>A	ENSP00000419838.1:n.180+807C>A
ENST00000494453.1:c.69+101C>A
NM_000187.3:c.649+101C>A	NP_000178.2:n.649+101C>A
XM_005247412.1:c.549+807C>A	XP_005247469.1:n.549+807C>A
XM_005247413.1:c.649+101C>A	XP_005247470.1:n.649+101C>A
XM_005247414.3:c.649+101C>A	XP_005247471.1:n.649+101C>A
XM_011512746.1:c.649+101C>A	XP_011511048.1:n.649+101C>A
XM_005247412.2:c.549+807C>A	XP_005247469.1:n.549+807C>A
XM_005247413.2:c.649+101C>A	XP_005247470.1:n.649+101C>A
XM_005247414.5:c.649+101C>A	XP_005247471.1:n.649+101C>A
XM_011512746.2:c.649+101C>A	XP_011511048.1:n.649+101C>A
XM_017006277.2:c.226+101C>A	XP_016861766.1:n.226+101C>A
NM_000187.4:c.649+101C>A MANE Select	NP_000178.2:n.649+101C>A