Canonical Allele Identifier: CA2667170997

Gene: HGD

Linked Data

• gnomAD v4: 3-120638328-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120638329del , CM000665.2:g.120638329del	GRCh38
NC_000003.11:g.120357176del , CM000665.1:g.120357176del	GRCh37
NC_000003.10:g.121839866del	NCBI36
NG_011957.1:g.49153del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.1006+126del MANE Select	ENSP00000283871.5:n.1006+126del
ENST00000283871.9:c.1006+126del	ENSP00000283871.5:n.1006+126del
ENST00000470321.1:n.346+126del
ENST00000475447.2:c.307+3260del
ENST00000492108.5:c.285+3260del	ENSP00000419838.1:n.285+3260del
ENST00000494453.1:c.426+126del
NM_000187.3:c.1006+126del	NP_000178.2:n.1006+126del
XM_005247412.1:c.781+126del	XP_005247469.1:n.781+126del
XM_005247413.1:c.1006+126del	XP_005247470.1:n.1006+126del
XM_011512746.1:c.879+3260del	XP_011511048.1:n.879+3260del
XM_005247412.2:c.781+126del	XP_005247469.1:n.781+126del
XM_005247413.2:c.1006+126del	XP_005247470.1:n.1006+126del
XM_011512746.2:c.879+3260del	XP_011511048.1:n.879+3260del
XM_017006277.2:c.583+126del	XP_016861766.1:n.583+126del
NM_000187.4:c.1006+126del MANE Select	NP_000178.2:n.1006+126del