Canonical Allele Identifier: CA2394917321
Gene: IL17RA HGNC NCBI

Linked Data

dbSNP Id: rs1337407803

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085077G>A , CM000684.2:g.17085077G>A GRCh38
NC_000022.10:g.17565967G>A , CM000684.1:g.17565967G>A GRCh37
NC_000022.9:g.15945967G>A NCBI36
NG_028257.1:g.5117G>A , LRG_355:g.5117G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000694948.1:n.84G>A
ENST00000694949.1:n.81G>A
ENST00000694950.1:c.66G>A
ENST00000319363.11:c.-15G>A MANE Select ENSP00000320936.6:n.-15G>A
ENST00000319363.10:c.-15G>A ENSP00000320936.6:n.-15G>A
ENST00000459971.1:n.21G>A
ENST00000477874.1:n.124G>A
ENST00000612619.1:c.-15G>A ENSP00000479970.1:n.-15G>A
NM_001289905.1:c.-15G>A NP_001276834.1:n.-15G>A
NM_014339.6:c.-15G>A , LRG_355t1:c.-15G>A NP_055154.3:n.-15G>A
NM_014339.7:c.-15G>A MANE Select NP_055154.3:n.-15G>A
NM_001289905.2:c.-15G>A NP_001276834.1:n.-15G>A