Canonical Allele Identifier: CA1397096498
Gene: HGD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120646172G= , CM000665.2:g.120646172G= GRCh38
NC_000003.11:g.120365019G= , CM000665.1:g.120365019G= GRCh37
NC_000003.10:g.121847709G= NCBI36
NG_011957.1:g.41310C=

Transcript Alleles

HGVS Amino-acid change
ENST00000283871.10:c.649+95C= MANE Select ENSP00000283871.5:n.649+95C=
ENST00000283871.9:c.649+95C= ENSP00000283871.5:n.649+95C=
ENST00000475447.2:c.180+95C=
ENST00000492108.5:c.180+801C= ENSP00000419838.1:n.180+801C=
ENST00000494453.1:c.69+95C=
NM_000187.3:c.649+95C= NP_000178.2:n.649+95C=
XM_005247412.1:c.549+801C= XP_005247469.1:n.549+801C=
XM_005247413.1:c.649+95C= XP_005247470.1:n.649+95C=
XM_005247414.3:c.649+95C= XP_005247471.1:n.649+95C=
XM_011512746.1:c.649+95C= XP_011511048.1:n.649+95C=
XM_005247412.2:c.549+801C= XP_005247469.1:n.549+801C=
XM_005247413.2:c.649+95C= XP_005247470.1:n.649+95C=
XM_005247414.5:c.649+95C= XP_005247471.1:n.649+95C=
XM_011512746.2:c.649+95C= XP_011511048.1:n.649+95C=
XM_017006277.2:c.226+95C= XP_016861766.1:n.226+95C=
NM_000187.4:c.649+95C= MANE Select NP_000178.2:n.649+95C=