Canonical Allele Identifier: CA2394917286
Gene: IL17RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085039T= , CM000684.2:g.17085039T= GRCh38
NC_000022.10:g.17565929T= , CM000684.1:g.17565929T= GRCh37
NC_000022.9:g.15945929T= NCBI36
NG_028257.1:g.5079T= , LRG_355:g.5079T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000694948.1:n.46T=
ENST00000694949.1:n.43T=
ENST00000694950.1:c.28T=
ENST00000319363.11:c.-53T= MANE Select ENSP00000320936.6:n.-53T=
ENST00000319363.10:c.-53T= ENSP00000320936.6:n.-53T=
ENST00000477874.1:n.86T=
ENST00000612619.1:c.-53T= ENSP00000479970.1:n.-53T=
NM_001289905.1:c.-53T= NP_001276834.1:n.-53T=
NM_014339.6:c.-53T= , LRG_355t1:c.-53T= NP_055154.3:n.-53T=
NM_014339.7:c.-53T= MANE Select NP_055154.3:n.-53T=
NM_001289905.2:c.-53T= NP_001276834.1:n.-53T=