Canonical Allele Identifier: CA410210257
Gene: IL17RA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085201A>C , CM000684.2:g.17085201A>C GRCh38
NC_000022.10:g.17566091A>C , CM000684.1:g.17566091A>C GRCh37
NC_000022.9:g.15946091A>C NCBI36
NG_028257.1:g.5241A>C , LRG_355:g.5241A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000612619.2:c.110A>C ENSP00000479970.1:p.Asp37Ala
ENST00000694948.1:n.208A>C
ENST00000694949.1:n.205A>C
ENST00000694950.1:c.190A>C
ENST00000319363.11:c.110A>C MANE Select ENSP00000320936.6:p.Asp37Ala
ENST00000319363.10:c.110A>C ENSP00000320936.6:p.Asp37Ala
ENST00000459971.1:n.145A>C
ENST00000477874.1:n.248A>C
ENST00000612619.1:c.110A>C ENSP00000479970.1:p.Asp37Ala
NM_001289905.1:c.110A>C NP_001276834.1:p.Asp37Ala
NM_014339.6:c.110A>C , LRG_355t1:c.110A>C NP_055154.3:p.Asp37Ala
NM_014339.7:c.110A>C MANE Select NP_055154.3:p.Asp37Ala
NM_001289905.2:c.110A>C NP_001276834.1:p.Asp37Ala