Canonical Allele Identifier: CA410210211
Gene: IL17RA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085177G>A , CM000684.2:g.17085177G>A GRCh38
NC_000022.10:g.17566067G>A , CM000684.1:g.17566067G>A GRCh37
NC_000022.9:g.15946067G>A NCBI36
NG_028257.1:g.5217G>A , LRG_355:g.5217G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000612619.2:c.86G>A ENSP00000479970.1:p.Gly29Asp
ENST00000694948.1:n.184G>A
ENST00000694949.1:n.181G>A
ENST00000694950.1:c.166G>A
ENST00000319363.11:c.86G>A MANE Select ENSP00000320936.6:p.Gly29Asp
ENST00000319363.10:c.86G>A ENSP00000320936.6:p.Gly29Asp
ENST00000459971.1:n.121G>A
ENST00000477874.1:n.224G>A
ENST00000612619.1:c.86G>A ENSP00000479970.1:p.Gly29Asp
NM_001289905.1:c.86G>A NP_001276834.1:p.Gly29Asp
NM_014339.6:c.86G>A , LRG_355t1:c.86G>A NP_055154.3:p.Gly29Asp
NM_014339.7:c.86G>A MANE Select NP_055154.3:p.Gly29Asp
NM_001289905.2:c.86G>A NP_001276834.1:p.Gly29Asp