Canonical Allele Identifier: CA638274545
Gene: IL17RA HGNC NCBI

Linked Data

dbSNP Id: rs1363057298

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085048G>A , CM000684.2:g.17085048G>A GRCh38
NC_000022.10:g.17565938G>A , CM000684.1:g.17565938G>A GRCh37
NC_000022.9:g.15945938G>A NCBI36
NG_028257.1:g.5088G>A , LRG_355:g.5088G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000694948.1:n.55G>A
ENST00000694949.1:n.52G>A
ENST00000694950.1:c.37G>A
ENST00000319363.11:c.-44G>A MANE Select ENSP00000320936.6:n.-44G>A
ENST00000319363.10:c.-44G>A ENSP00000320936.6:n.-44G>A
ENST00000477874.1:n.95G>A
ENST00000612619.1:c.-44G>A ENSP00000479970.1:n.-44G>A
NM_001289905.1:c.-44G>A NP_001276834.1:n.-44G>A
NM_014339.6:c.-44G>A , LRG_355t1:c.-44G>A NP_055154.3:n.-44G>A
NM_014339.7:c.-44G>A MANE Select NP_055154.3:n.-44G>A
NM_001289905.2:c.-44G>A NP_001276834.1:n.-44G>A