Canonical Allele Identifier: CA354081201
Community Standard Title: NM_000187.4(HGD):c.255G>A (p.Trp85Ter)
Gene: HGD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120670454C>T , CM000665.2:g.120670454C>T GRCh38
NC_000003.11:g.120389301C>T , CM000665.1:g.120389301C>T GRCh37
NC_000003.10:g.121871991C>T NCBI36
NG_011957.1:g.17028G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000187.4:c.255G>A MANE Select NP_000178.2:p.Trp85Ter
ENST00000283871.10:c.255G>A MANE Select ENSP00000283871.5:p.Trp85Ter
NM_000187.3:c.255G>A NP_000178.2:p.Trp85Ter
ENST00000283871.9:c.255G>A ENSP00000283871.5:p.Trp85Ter
ENST00000466528.5:n.281G>A
ENST00000476082.2:c.132G>A ENSP00000419560.2:p.Trp44Ter
ENST00000485313.5:n.363G>A
ENST00000488183.5:n.513G>A
XM_005247412.1:c.255G>A XP_005247469.1:p.Trp85Ter
XM_005247412.2:c.255G>A XP_005247469.1:p.Trp85Ter
XM_005247413.1:c.255G>A XP_005247470.1:p.Trp85Ter
XM_005247413.2:c.255G>A XP_005247470.1:p.Trp85Ter
XM_005247414.3:c.255G>A XP_005247471.1:p.Trp85Ter
XM_005247414.5:c.255G>A XP_005247471.1:p.Trp85Ter
XM_011512746.1:c.255G>A XP_011511048.1:p.Trp85Ter
XM_011512746.2:c.255G>A XP_011511048.1:p.Trp85Ter
XM_017006277.2:c.-169G>A XP_016861766.1:n.-169G>A