Canonical Allele Identifier: CA2394917458
Gene: IL17RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085262G= , CM000684.2:g.17085262G= GRCh38
NC_000022.10:g.17566152G= , CM000684.1:g.17566152G= GRCh37
NC_000022.9:g.15946152G= NCBI36
NG_028257.1:g.5302G= , LRG_355:g.5302G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000612619.2:c.138+33G= ENSP00000479970.1:n.138+33G=
ENST00000694948.1:n.236+33G=
ENST00000694949.1:n.233+33G=
ENST00000694950.1:c.218+33G=
ENST00000319363.11:c.138+33G= MANE Select ENSP00000320936.6:n.138+33G=
ENST00000319363.10:c.138+33G= ENSP00000320936.6:n.138+33G=
ENST00000459971.1:n.173+33G=
ENST00000477874.1:n.276+33G=
ENST00000612619.1:c.138+33G= ENSP00000479970.1:n.138+33G=
NM_001289905.1:c.138+33G= NP_001276834.1:n.138+33G=
NM_014339.6:c.138+33G= , LRG_355t1:c.138+33G= NP_055154.3:n.138+33G=
NM_014339.7:c.138+33G= MANE Select NP_055154.3:n.138+33G=
NM_001289905.2:c.138+33G= NP_001276834.1:n.138+33G=