Canonical Allele Identifier: CA354078059
Gene: HGD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120650814C>A , CM000665.2:g.120650814C>A GRCh38
NC_000003.11:g.120369661C>A , CM000665.1:g.120369661C>A GRCh37
NC_000003.10:g.121852351C>A NCBI36
NG_011957.1:g.36668G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000283871.10:c.394G>T MANE Select ENSP00000283871.5:p.Ala132Ser
ENST00000283871.9:c.394G>T ENSP00000283871.5:p.Ala132Ser
ENST00000476082.2:c.271G>T ENSP00000419560.2:p.Ala91Ser
ENST00000485313.5:n.502G>T
ENST00000492108.5:c.25G>T ENSP00000419838.1:p.Ala9Ser
NM_000187.3:c.394G>T NP_000178.2:p.Ala132Ser
XM_005247412.1:c.394G>T XP_005247469.1:p.Ala132Ser
XM_005247413.1:c.394G>T XP_005247470.1:p.Ala132Ser
XM_005247414.3:c.394G>T XP_005247471.1:p.Ala132Ser
XM_011512746.1:c.394G>T XP_011511048.1:p.Ala132Ser
XM_005247412.2:c.394G>T XP_005247469.1:p.Ala132Ser
XM_005247413.2:c.394G>T XP_005247470.1:p.Ala132Ser
XM_005247414.5:c.394G>T XP_005247471.1:p.Ala132Ser
XM_011512746.2:c.394G>T XP_011511048.1:p.Ala132Ser
XM_017006277.2:c.-30G>T XP_016861766.1:n.-30G>T
NM_000187.4:c.394G>T MANE Select NP_000178.2:p.Ala132Ser