Canonical Allele Identifier: CA2394917441
Gene: IL17RA HGNC NCBI

Linked Data

dbSNP Id: rs1412741494

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085247dup , CM000684.2:g.17085247dup GRCh38
NC_000022.10:g.17566137dup , CM000684.1:g.17566137dup GRCh37
NC_000022.9:g.15946137dup NCBI36
NG_028257.1:g.5287dup , LRG_355:g.5287dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000612619.2:c.138+18dup ENSP00000479970.1:n.138+18dup
ENST00000694948.1:n.236+18dup
ENST00000694949.1:n.233+18dup
ENST00000694950.1:c.218+18dup
ENST00000319363.11:c.138+18dup MANE Select ENSP00000320936.6:n.138+18dup
ENST00000319363.10:c.138+18dup ENSP00000320936.6:n.138+18dup
ENST00000459971.1:n.173+18dup
ENST00000477874.1:n.276+18dup
ENST00000612619.1:c.138+18dup ENSP00000479970.1:n.138+18dup
NM_001289905.1:c.138+18dup NP_001276834.1:n.138+18dup
NM_014339.6:c.138+18dup , LRG_355t1:c.138+18dup NP_055154.3:n.138+18dup
NM_014339.7:c.138+18dup MANE Select NP_055154.3:n.138+18dup
NM_001289905.2:c.138+18dup NP_001276834.1:n.138+18dup