Canonical Allele Identifier: CA2667173125

Gene: HGD

Linked Data

• gnomAD v4: 3-120675045-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120675048del , CM000665.2:g.120675048del	GRCh38
NC_000003.11:g.120393895del , CM000665.1:g.120393895del	GRCh37
NC_000003.10:g.121876585del	NCBI36
NG_011957.1:g.12436del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.88-57del MANE Select	ENSP00000283871.5:n.88-57del
ENST00000283871.9:c.88-57del	ENSP00000283871.5:n.88-57del
ENST00000466528.5:n.114-57del
ENST00000476082.2:c.53+746del	ENSP00000419560.2:n.53+746del
ENST00000480862.1:n.246-57del
ENST00000485313.5:n.196-57del
ENST00000488183.5:n.346-57del
NM_000187.3:c.88-57del	NP_000178.2:n.88-57del
XM_005247412.1:c.88-57del	XP_005247469.1:n.88-57del
XM_005247413.1:c.88-57del	XP_005247470.1:n.88-57del
XM_005247414.3:c.88-57del	XP_005247471.1:n.88-57del
XM_011512746.1:c.88-57del	XP_011511048.1:n.88-57del
XM_005247412.2:c.88-57del	XP_005247469.1:n.88-57del
XM_005247413.2:c.88-57del	XP_005247470.1:n.88-57del
XM_005247414.5:c.88-57del	XP_005247471.1:n.88-57del
XM_011512746.2:c.88-57del	XP_011511048.1:n.88-57del
XM_017006277.2:c.-336-57del	XP_016861766.1:n.-336-57del
NM_000187.4:c.88-57del MANE Select	NP_000178.2:n.88-57del