Canonical Allele Identifier: CA354077969

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120650775T>A , CM000665.2:g.120650775T>A	GRCh38
NC_000003.11:g.120369622T>A , CM000665.1:g.120369622T>A	GRCh37
NC_000003.10:g.121852312T>A	NCBI36
NG_011957.1:g.36707A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000187.4:c.433A>T MANE Select	NP_000178.2:p.Arg145Ter
ENST00000283871.10:c.433A>T MANE Select	ENSP00000283871.5:p.Arg145Ter
NM_000187.3:c.433A>T	NP_000178.2:p.Arg145Ter
ENST00000283871.9:c.433A>T	ENSP00000283871.5:p.Arg145Ter
ENST00000476082.2:c.310A>T	ENSP00000419560.2:p.Arg104Ter
ENST00000492108.5:c.64A>T	ENSP00000419838.1:p.Arg22Ter
XM_005247412.1:c.433A>T	XP_005247469.1:p.Arg145Ter
XM_005247412.2:c.433A>T	XP_005247469.1:p.Arg145Ter
XM_005247413.1:c.433A>T	XP_005247470.1:p.Arg145Ter
XM_005247413.2:c.433A>T	XP_005247470.1:p.Arg145Ter
XM_005247414.3:c.433A>T	XP_005247471.1:p.Arg145Ter
XM_005247414.5:c.433A>T	XP_005247471.1:p.Arg145Ter
XM_011512746.1:c.433A>T	XP_011511048.1:p.Arg145Ter
XM_011512746.2:c.433A>T	XP_011511048.1:p.Arg145Ter
XM_017006277.2:c.10A>T	XP_016861766.1:p.Arg4Ter