Canonical Allele Identifier: CA410210284
Gene: IL17RA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085215G>T , CM000684.2:g.17085215G>T GRCh38
NC_000022.10:g.17566105G>T , CM000684.1:g.17566105G>T GRCh37
NC_000022.9:g.15946105G>T NCBI36
NG_028257.1:g.5255G>T , LRG_355:g.5255G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000612619.2:c.124G>T ENSP00000479970.1:p.Val42Phe
ENST00000694948.1:n.222G>T
ENST00000694949.1:n.219G>T
ENST00000694950.1:c.204G>T
ENST00000319363.11:c.124G>T MANE Select ENSP00000320936.6:p.Val42Phe
ENST00000319363.10:c.124G>T ENSP00000320936.6:p.Val42Phe
ENST00000459971.1:n.159G>T
ENST00000477874.1:n.262G>T
ENST00000612619.1:c.124G>T ENSP00000479970.1:p.Val42Phe
NM_001289905.1:c.124G>T NP_001276834.1:p.Val42Phe
NM_014339.6:c.124G>T , LRG_355t1:c.124G>T NP_055154.3:p.Val42Phe
NM_014339.7:c.124G>T MANE Select NP_055154.3:p.Val42Phe
NM_001289905.2:c.124G>T NP_001276834.1:p.Val42Phe