Canonical Allele Identifier: CA354077044

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120647014C>T , CM000665.2:g.120647014C>T	GRCh38
NC_000003.11:g.120365861C>T , CM000665.1:g.120365861C>T	GRCh37
NC_000003.10:g.121848551C>T	NCBI36
NG_011957.1:g.40468G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000187.4:c.508G>A MANE Select	NP_000178.2:p.Gly170Ser
ENST00000283871.10:c.508G>A MANE Select	ENSP00000283871.5:p.Gly170Ser
NM_000187.3:c.508G>A	NP_000178.2:p.Gly170Ser
ENST00000283871.9:c.508G>A	ENSP00000283871.5:p.Gly170Ser
ENST00000475447.2:c.39G>A
ENST00000476082.2:c.385G>A	ENSP00000419560.2:p.Gly129Ser
ENST00000492108.5:c.139G>A	ENSP00000419838.1:p.Gly47Ser
XM_005247412.1:c.508G>A	XP_005247469.1:p.Gly170Ser
XM_005247412.2:c.508G>A	XP_005247469.1:p.Gly170Ser
XM_005247413.1:c.508G>A	XP_005247470.1:p.Gly170Ser
XM_005247413.2:c.508G>A	XP_005247470.1:p.Gly170Ser
XM_005247414.3:c.508G>A	XP_005247471.1:p.Gly170Ser
XM_005247414.5:c.508G>A	XP_005247471.1:p.Gly170Ser
XM_011512746.1:c.508G>A	XP_011511048.1:p.Gly170Ser
XM_011512746.2:c.508G>A	XP_011511048.1:p.Gly170Ser
XM_017006277.2:c.85G>A	XP_016861766.1:p.Gly29Ser