Canonical Allele Identifier: CA1397107408
Gene: HGD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120670551A= , CM000665.2:g.120670551A= GRCh38
NC_000003.11:g.120389398A= , CM000665.1:g.120389398A= GRCh37
NC_000003.10:g.121872088A= NCBI36
NG_011957.1:g.16931T=

Transcript Alleles

HGVS Amino-acid change
ENST00000283871.10:c.177-19T= MANE Select ENSP00000283871.5:n.177-19T=
ENST00000283871.9:c.177-19T= ENSP00000283871.5:n.177-19T=
ENST00000466528.5:n.203-19T=
ENST00000476082.2:c.54-19T= ENSP00000419560.2:n.54-19T=
ENST00000485313.5:n.285-19T=
ENST00000488183.5:n.435-19T=
NM_000187.3:c.177-19T= NP_000178.2:n.177-19T=
XM_005247412.1:c.177-19T= XP_005247469.1:n.177-19T=
XM_005247413.1:c.177-19T= XP_005247470.1:n.177-19T=
XM_005247414.3:c.177-19T= XP_005247471.1:n.177-19T=
XM_011512746.1:c.177-19T= XP_011511048.1:n.177-19T=
XM_005247412.2:c.177-19T= XP_005247469.1:n.177-19T=
XM_005247413.2:c.177-19T= XP_005247470.1:n.177-19T=
XM_005247414.5:c.177-19T= XP_005247471.1:n.177-19T=
XM_011512746.2:c.177-19T= XP_011511048.1:n.177-19T=
XM_017006277.2:c.-247-19T= XP_016861766.1:n.-247-19T=
NM_000187.4:c.177-19T= MANE Select NP_000178.2:n.177-19T=