Canonical Allele Identifier: CA2394923238
Gene: IL17RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17097840C= , CM000684.2:g.17097840C= GRCh38
NC_000022.10:g.17578730C= , CM000684.1:g.17578730C= GRCh37
NC_000022.9:g.15958730C= NCBI36
NG_028257.1:g.17880C= , LRG_355:g.17880C=

Transcript Alleles

HGVS Amino-acid change
ENST00000612619.2:c.207C= ENSP00000479970.1:p.Thr69=
ENST00000694948.1:n.305C=
ENST00000694949.1:n.302C=
ENST00000694950.1:c.244-16C=
ENST00000694951.1:n.70C=
ENST00000319363.11:c.207C= MANE Select ENSP00000320936.6:p.Thr69=
ENST00000319363.10:c.207C= ENSP00000320936.6:p.Thr69=
ENST00000477874.1:n.320C=
ENST00000612619.1:c.207C= ENSP00000479970.1:p.Thr69=
NM_001289905.1:c.207C= NP_001276834.1:p.Thr69=
NM_014339.6:c.207C= , LRG_355t1:c.207C= NP_055154.3:p.Thr69=
NM_014339.7:c.207C= MANE Select NP_055154.3:p.Thr69=
NM_001289905.2:c.207C= NP_001276834.1:p.Thr69=