Canonical Allele Identifier: CA354073624

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120638535C>A , CM000665.2:g.120638535C>A	GRCh38
NC_000003.11:g.120357382C>A , CM000665.1:g.120357382C>A	GRCh37
NC_000003.10:g.121840072C>A	NCBI36
NG_011957.1:g.48947G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000187.4:c.926G>T MANE Select	NP_000178.2:p.Gly309Val
ENST00000283871.10:c.926G>T MANE Select	ENSP00000283871.5:p.Gly309Val
NM_000187.3:c.926G>T	NP_000178.2:p.Gly309Val
ENST00000283871.9:c.926G>T	ENSP00000283871.5:p.Gly309Val
ENST00000470321.1:n.266G>T
ENST00000475447.2:c.307+3054G>T
ENST00000492108.5:c.285+3054G>T	ENSP00000419838.1:n.285+3054G>T
ENST00000494453.1:c.346G>T
XM_005247412.1:c.701G>T	XP_005247469.1:p.Gly234Val
XM_005247412.2:c.701G>T	XP_005247469.1:p.Gly234Val
XM_005247413.1:c.926G>T	XP_005247470.1:p.Gly309Val
XM_005247413.2:c.926G>T	XP_005247470.1:p.Gly309Val
XM_011512746.1:c.879+3054G>T	XP_011511048.1:n.879+3054G>T
XM_011512746.2:c.879+3054G>T	XP_011511048.1:n.879+3054G>T
XM_017006277.2:c.503G>T	XP_016861766.1:p.Gly168Val