Canonical Allele Identifier: CA354076949

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120646990C>A , CM000665.2:g.120646990C>A	GRCh38
NC_000003.11:g.120365837C>A , CM000665.1:g.120365837C>A	GRCh37
NC_000003.10:g.121848527C>A	NCBI36
NG_011957.1:g.40492G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000187.4:c.532G>T MANE Select	NP_000178.2:p.Glu178Ter
ENST00000283871.10:c.532G>T MANE Select	ENSP00000283871.5:p.Glu178Ter
NM_000187.3:c.532G>T	NP_000178.2:p.Glu178Ter
ENST00000283871.9:c.532G>T	ENSP00000283871.5:p.Glu178Ter
ENST00000475447.2:c.63G>T
ENST00000476082.2:c.409G>T	ENSP00000419560.2:p.Glu137Ter
ENST00000492108.5:c.163G>T	ENSP00000419838.1:p.Glu55Ter
XM_005247412.1:c.532G>T	XP_005247469.1:p.Glu178Ter
XM_005247412.2:c.532G>T	XP_005247469.1:p.Glu178Ter
XM_005247413.1:c.532G>T	XP_005247470.1:p.Glu178Ter
XM_005247413.2:c.532G>T	XP_005247470.1:p.Glu178Ter
XM_005247414.3:c.532G>T	XP_005247471.1:p.Glu178Ter
XM_005247414.5:c.532G>T	XP_005247471.1:p.Glu178Ter
XM_011512746.1:c.532G>T	XP_011511048.1:p.Glu178Ter
XM_011512746.2:c.532G>T	XP_011511048.1:p.Glu178Ter
XM_017006277.2:c.109G>T	XP_016861766.1:p.Glu37Ter