Canonical Allele Identifier: CA1367043775
Gene: IL17RD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.57106133G= , CM000665.2:g.57106133G= GRCh38
NC_000003.11:g.57140161G= , CM000665.1:g.57140161G= GRCh37
NC_000003.10:g.57115201G= NCBI36
NG_047158.1:g.69185C=

Transcript Alleles

HGVS Amino-acid change
ENST00000296318.12:c.572C= MANE Select ENSP00000296318.7:p.Pro191=
ENST00000296318.11:c.572C= ENSP00000296318.7:p.Pro191=
ENST00000320057.9:c.140C= ENSP00000322250.5:p.Pro47=
ENST00000463523.5:c.140C= ENSP00000417516.1:p.Pro47=
ENST00000467210.5:c.140C= ENSP00000418368.1:p.Pro47=
ENST00000469841.5:n.509C=
NM_017563.3:c.572C= NP_060033.3:p.Pro191=
XM_005265238.3:c.488C= XP_005265295.1:p.Pro163=
XM_006713209.2:c.140C= XP_006713272.1:p.Pro47=
XM_011533849.1:c.500C= XP_011532151.1:p.Pro167=
XM_011533850.1:c.140C= XP_011532152.1:p.Pro47=
NM_001318864.1:c.140C= NP_001305793.1:p.Pro47=
NM_017563.4:c.572C= NP_060033.3:p.Pro191=
XM_005265238.4:c.488C= XP_005265295.1:p.Pro163=
XM_011533849.2:c.140C= XP_011532151.2:p.Pro47=
NM_017563.5:c.572C= MANE Select NP_060033.3:p.Pro191=
NM_001318864.2:c.140C= NP_001305793.1:p.Pro47=