Canonical Allele Identifier: CA1397099330
Gene: HGD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120652507C= , CM000665.2:g.120652507C= GRCh38
NC_000003.11:g.120371354C= , CM000665.1:g.120371354C= GRCh37
NC_000003.10:g.121854044C= NCBI36
NG_011957.1:g.34975G=

Transcript Alleles

HGVS Amino-acid change
ENST00000283871.10:c.342+85G= MANE Select ENSP00000283871.5:n.342+85G=
ENST00000283871.9:c.342+85G= ENSP00000283871.5:n.342+85G=
ENST00000476082.2:c.219+85G= ENSP00000419560.2:n.219+85G=
ENST00000485313.5:n.450+85G=
NM_000187.3:c.342+85G= NP_000178.2:n.342+85G=
XM_005247412.1:c.342+85G= XP_005247469.1:n.342+85G=
XM_005247413.1:c.342+85G= XP_005247470.1:n.342+85G=
XM_005247414.3:c.342+85G= XP_005247471.1:n.342+85G=
XM_011512746.1:c.342+85G= XP_011511048.1:n.342+85G=
XM_005247412.2:c.342+85G= XP_005247469.1:n.342+85G=
XM_005247413.2:c.342+85G= XP_005247470.1:n.342+85G=
XM_005247414.5:c.342+85G= XP_005247471.1:n.342+85G=
XM_011512746.2:c.342+85G= XP_011511048.1:n.342+85G=
XM_017006277.2:c.-82+85G= XP_016861766.1:n.-82+85G=
NM_000187.4:c.342+85G= MANE Select NP_000178.2:n.342+85G=