Canonical Allele Identifier: CA2667172338

Gene: HGD

Linked Data

• gnomAD v4: 3-120652512-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120652512C>T , CM000665.2:g.120652512C>T	GRCh38
NC_000003.11:g.120371359C>T , CM000665.1:g.120371359C>T	GRCh37
NC_000003.10:g.121854049C>T	NCBI36
NG_011957.1:g.34970G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.342+80G>A MANE Select	ENSP00000283871.5:n.342+80G>A
ENST00000283871.9:c.342+80G>A	ENSP00000283871.5:n.342+80G>A
ENST00000476082.2:c.219+80G>A	ENSP00000419560.2:n.219+80G>A
ENST00000485313.5:n.450+80G>A
NM_000187.3:c.342+80G>A	NP_000178.2:n.342+80G>A
XM_005247412.1:c.342+80G>A	XP_005247469.1:n.342+80G>A
XM_005247413.1:c.342+80G>A	XP_005247470.1:n.342+80G>A
XM_005247414.3:c.342+80G>A	XP_005247471.1:n.342+80G>A
XM_011512746.1:c.342+80G>A	XP_011511048.1:n.342+80G>A
XM_005247412.2:c.342+80G>A	XP_005247469.1:n.342+80G>A
XM_005247413.2:c.342+80G>A	XP_005247470.1:n.342+80G>A
XM_005247414.5:c.342+80G>A	XP_005247471.1:n.342+80G>A
XM_011512746.2:c.342+80G>A	XP_011511048.1:n.342+80G>A
XM_017006277.2:c.-82+80G>A	XP_016861766.1:n.-82+80G>A
NM_000187.4:c.342+80G>A MANE Select	NP_000178.2:n.342+80G>A