Canonical Allele Identifier: CA354078143
Gene: HGD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120650856T>C , CM000665.2:g.120650856T>C GRCh38
NC_000003.11:g.120369703T>C , CM000665.1:g.120369703T>C GRCh37
NC_000003.10:g.121852393T>C NCBI36
NG_011957.1:g.36626A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000283871.10:c.352A>G MANE Select ENSP00000283871.5:p.Thr118Ala
ENST00000283871.9:c.352A>G ENSP00000283871.5:p.Thr118Ala
ENST00000476082.2:c.229A>G ENSP00000419560.2:p.Thr77Ala
ENST00000485313.5:n.460A>G
NM_000187.3:c.352A>G NP_000178.2:p.Thr118Ala
XM_005247412.1:c.352A>G XP_005247469.1:p.Thr118Ala
XM_005247413.1:c.352A>G XP_005247470.1:p.Thr118Ala
XM_005247414.3:c.352A>G XP_005247471.1:p.Thr118Ala
XM_011512746.1:c.352A>G XP_011511048.1:p.Thr118Ala
XM_005247412.2:c.352A>G XP_005247469.1:p.Thr118Ala
XM_005247413.2:c.352A>G XP_005247470.1:p.Thr118Ala
XM_005247414.5:c.352A>G XP_005247471.1:p.Thr118Ala
XM_011512746.2:c.352A>G XP_011511048.1:p.Thr118Ala
XM_017006277.2:c.-72A>G XP_016861766.1:n.-72A>G
NM_000187.4:c.352A>G MANE Select NP_000178.2:p.Thr118Ala