Canonical Allele Identifier: CA143831
Gene: IL17RD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.57098300G>A , CM000665.2:g.57098300G>A GRCh38
NC_000003.11:g.57132328G>A , CM000665.1:g.57132328G>A GRCh37
NC_000003.10:g.57107368G>A NCBI36
NG_047158.1:g.77018C>T

Transcript Alleles

HGVS Amino-acid Change
NM_017563.5:c.1403C>T MANE Select NP_060033.3:p.Ser468Leu
ENST00000296318.12:c.1403C>T MANE Select ENSP00000296318.7:p.Ser468Leu
NM_001318864.1:c.971C>T NP_001305793.1:p.Ser324Leu
NM_001318864.2:c.971C>T NP_001305793.1:p.Ser324Leu
NM_017563.3:c.1403C>T NP_060033.3:p.Ser468Leu
NM_017563.4:c.1403C>T NP_060033.3:p.Ser468Leu
ENST00000296318.11:c.1403C>T ENSP00000296318.7:p.Ser468Leu
ENST00000320057.9:c.971C>T ENSP00000322250.5:p.Ser324Leu
ENST00000463523.5:c.971C>T ENSP00000417516.1:p.Ser324Leu
ENST00000469841.5:n.1340C>T
XM_005265238.3:c.1319C>T XP_005265295.1:p.Ser440Leu
XM_005265238.4:c.1319C>T XP_005265295.1:p.Ser440Leu
XM_006713209.2:c.971C>T XP_006713272.1:p.Ser324Leu
XM_011533849.1:c.1331C>T XP_011532151.1:p.Ser444Leu
XM_011533849.2:c.971C>T XP_011532151.2:p.Ser324Leu
XM_011533850.1:c.971C>T XP_011532152.1:p.Ser324Leu