Canonical Allele Identifier: CA1367043777
Gene: IL17RD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.57106137G= , CM000665.2:g.57106137G= GRCh38
NC_000003.11:g.57140165G= , CM000665.1:g.57140165G= GRCh37
NC_000003.10:g.57115205G= NCBI36
NG_047158.1:g.69181C=

Transcript Alleles

HGVS Amino-acid change
ENST00000296318.12:c.568C= MANE Select ENSP00000296318.7:p.Gln190=
ENST00000296318.11:c.568C= ENSP00000296318.7:p.Gln190=
ENST00000320057.9:c.136C= ENSP00000322250.5:p.Gln46=
ENST00000463523.5:c.136C= ENSP00000417516.1:p.Gln46=
ENST00000467210.5:c.136C= ENSP00000418368.1:p.Gln46=
ENST00000469841.5:n.505C=
NM_017563.3:c.568C= NP_060033.3:p.Gln190=
XM_005265238.3:c.484C= XP_005265295.1:p.Gln162=
XM_006713209.2:c.136C= XP_006713272.1:p.Gln46=
XM_011533849.1:c.496C= XP_011532151.1:p.Gln166=
XM_011533850.1:c.136C= XP_011532152.1:p.Gln46=
NM_001318864.1:c.136C= NP_001305793.1:p.Gln46=
NM_017563.4:c.568C= NP_060033.3:p.Gln190=
XM_005265238.4:c.484C= XP_005265295.1:p.Gln162=
XM_011533849.2:c.136C= XP_011532151.2:p.Gln46=
NM_017563.5:c.568C= MANE Select NP_060033.3:p.Gln190=
NM_001318864.2:c.136C= NP_001305793.1:p.Gln46=