Canonical Allele Identifier: CA354081450
Gene: HGD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120670498T>A , CM000665.2:g.120670498T>A GRCh38
NC_000003.11:g.120389345T>A , CM000665.1:g.120389345T>A GRCh37
NC_000003.10:g.121872035T>A NCBI36
NG_011957.1:g.16984A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000283871.10:c.211A>T MANE Select ENSP00000283871.5:p.Lys71Ter
ENST00000283871.9:c.211A>T ENSP00000283871.5:p.Lys71Ter
ENST00000466528.5:n.237A>T
ENST00000476082.2:c.88A>T ENSP00000419560.2:p.Lys30Ter
ENST00000485313.5:n.319A>T
ENST00000488183.5:n.469A>T
NM_000187.3:c.211A>T NP_000178.2:p.Lys71Ter
XM_005247412.1:c.211A>T XP_005247469.1:p.Lys71Ter
XM_005247413.1:c.211A>T XP_005247470.1:p.Lys71Ter
XM_005247414.3:c.211A>T XP_005247471.1:p.Lys71Ter
XM_011512746.1:c.211A>T XP_011511048.1:p.Lys71Ter
XM_005247412.2:c.211A>T XP_005247469.1:p.Lys71Ter
XM_005247413.2:c.211A>T XP_005247470.1:p.Lys71Ter
XM_005247414.5:c.211A>T XP_005247471.1:p.Lys71Ter
XM_011512746.2:c.211A>T XP_011511048.1:p.Lys71Ter
XM_017006277.2:c.-213A>T XP_016861766.1:n.-213A>T
NM_000187.4:c.211A>T MANE Select NP_000178.2:p.Lys71Ter