Canonical Allele Identifier: CA2667172632

Gene: HGD

Linked Data

• gnomAD v4: 3-120670395-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120670395A>G , CM000665.2:g.120670395A>G	GRCh38
NC_000003.11:g.120389242A>G , CM000665.1:g.120389242A>G	GRCh37
NC_000003.10:g.121871932A>G	NCBI36
NG_011957.1:g.17087T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.282+32T>C MANE Select	ENSP00000283871.5:n.282+32T>C
ENST00000283871.9:c.282+32T>C	ENSP00000283871.5:n.282+32T>C
ENST00000466528.5:n.340T>C
ENST00000476082.2:c.159+32T>C	ENSP00000419560.2:n.159+32T>C
ENST00000485313.5:n.390+32T>C
ENST00000488183.5:n.540+32T>C
NM_000187.3:c.282+32T>C	NP_000178.2:n.282+32T>C
XM_005247412.1:c.282+32T>C	XP_005247469.1:n.282+32T>C
XM_005247413.1:c.282+32T>C	XP_005247470.1:n.282+32T>C
XM_005247414.3:c.282+32T>C	XP_005247471.1:n.282+32T>C
XM_011512746.1:c.282+32T>C	XP_011511048.1:n.282+32T>C
XM_005247412.2:c.282+32T>C	XP_005247469.1:n.282+32T>C
XM_005247413.2:c.282+32T>C	XP_005247470.1:n.282+32T>C
XM_005247414.5:c.282+32T>C	XP_005247471.1:n.282+32T>C
XM_011512746.2:c.282+32T>C	XP_011511048.1:n.282+32T>C
XM_017006277.2:c.-142+32T>C	XP_016861766.1:n.-142+32T>C
NM_000187.4:c.282+32T>C MANE Select	NP_000178.2:n.282+32T>C