Canonical Allele Identifier: CA81781705

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120638563C>A , CM000665.2:g.120638563C>A	GRCh38
NC_000003.11:g.120357410C>A , CM000665.1:g.120357410C>A	GRCh37
NC_000003.10:g.121840100C>A	NCBI36
NG_011957.1:g.48919G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000187.4:c.898G>T MANE Select	NP_000178.2:p.Val300Leu
ENST00000283871.10:c.898G>T MANE Select	ENSP00000283871.5:p.Val300Leu
NM_000187.3:c.898G>T	NP_000178.2:p.Val300Leu
ENST00000283871.9:c.898G>T	ENSP00000283871.5:p.Val300Leu
ENST00000470321.1:n.238G>T
ENST00000475447.2:c.307+3026G>T
ENST00000492108.5:c.285+3026G>T	ENSP00000419838.1:n.285+3026G>T
ENST00000494453.1:c.318G>T
XM_005247412.1:c.673G>T	XP_005247469.1:p.Val225Leu
XM_005247412.2:c.673G>T	XP_005247469.1:p.Val225Leu
XM_005247413.1:c.898G>T	XP_005247470.1:p.Val300Leu
XM_005247413.2:c.898G>T	XP_005247470.1:p.Val300Leu
XM_011512746.1:c.879+3026G>T	XP_011511048.1:n.879+3026G>T
XM_011512746.2:c.879+3026G>T	XP_011511048.1:n.879+3026G>T
XM_017006277.2:c.475G>T	XP_016861766.1:p.Val159Leu