Canonical Allele Identifier: CA1397099329
Gene: HGD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120652505T= , CM000665.2:g.120652505T= GRCh38
NC_000003.11:g.120371352T= , CM000665.1:g.120371352T= GRCh37
NC_000003.10:g.121854042T= NCBI36
NG_011957.1:g.34977A=

Transcript Alleles

HGVS Amino-acid change
ENST00000283871.10:c.342+87A= MANE Select ENSP00000283871.5:n.342+87A=
ENST00000283871.9:c.342+87A= ENSP00000283871.5:n.342+87A=
ENST00000476082.2:c.219+87A= ENSP00000419560.2:n.219+87A=
ENST00000485313.5:n.450+87A=
NM_000187.3:c.342+87A= NP_000178.2:n.342+87A=
XM_005247412.1:c.342+87A= XP_005247469.1:n.342+87A=
XM_005247413.1:c.342+87A= XP_005247470.1:n.342+87A=
XM_005247414.3:c.342+87A= XP_005247471.1:n.342+87A=
XM_011512746.1:c.342+87A= XP_011511048.1:n.342+87A=
XM_005247412.2:c.342+87A= XP_005247469.1:n.342+87A=
XM_005247413.2:c.342+87A= XP_005247470.1:n.342+87A=
XM_005247414.5:c.342+87A= XP_005247471.1:n.342+87A=
XM_011512746.2:c.342+87A= XP_011511048.1:n.342+87A=
XM_017006277.2:c.-82+87A= XP_016861766.1:n.-82+87A=
NM_000187.4:c.342+87A= MANE Select NP_000178.2:n.342+87A=