Canonical Allele Identifier: CA2394917402
Gene: IL17RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085186C= , CM000684.2:g.17085186C= GRCh38
NC_000022.10:g.17566076C= , CM000684.1:g.17566076C= GRCh37
NC_000022.9:g.15946076C= NCBI36
NG_028257.1:g.5226C= , LRG_355:g.5226C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000612619.2:c.95C= ENSP00000479970.1:p.Ser32=
ENST00000694948.1:n.193C=
ENST00000694949.1:n.190C=
ENST00000694950.1:c.175C=
ENST00000319363.11:c.95C= MANE Select ENSP00000320936.6:p.Ser32=
ENST00000319363.10:c.95C= ENSP00000320936.6:p.Ser32=
ENST00000459971.1:n.130C=
ENST00000477874.1:n.233C=
ENST00000612619.1:c.95C= ENSP00000479970.1:p.Ser32=
NM_001289905.1:c.95C= NP_001276834.1:p.Ser32=
NM_014339.6:c.95C= , LRG_355t1:c.95C= NP_055154.3:p.Ser32=
NM_014339.7:c.95C= MANE Select NP_055154.3:p.Ser32=
NM_001289905.2:c.95C= NP_001276834.1:p.Ser32=