Canonical Allele Identifier: CA410210146
Gene: IL17RA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085140G>T , CM000684.2:g.17085140G>T GRCh38
NC_000022.10:g.17566030G>T , CM000684.1:g.17566030G>T GRCh37
NC_000022.9:g.15946030G>T NCBI36
NG_028257.1:g.5180G>T , LRG_355:g.5180G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000612619.2:c.49G>T ENSP00000479970.1:p.Gly17Trp
ENST00000694948.1:n.147G>T
ENST00000694949.1:n.144G>T
ENST00000694950.1:c.129G>T
ENST00000319363.11:c.49G>T MANE Select ENSP00000320936.6:p.Gly17Trp
ENST00000319363.10:c.49G>T ENSP00000320936.6:p.Gly17Trp
ENST00000459971.1:n.84G>T
ENST00000477874.1:n.187G>T
ENST00000612619.1:c.49G>T ENSP00000479970.1:p.Gly17Trp
NM_001289905.1:c.49G>T NP_001276834.1:p.Gly17Trp
NM_014339.6:c.49G>T , LRG_355t1:c.49G>T NP_055154.3:p.Gly17Trp
NM_014339.7:c.49G>T MANE Select NP_055154.3:p.Gly17Trp
NM_001289905.2:c.49G>T NP_001276834.1:p.Gly17Trp