Canonical Allele Identifier: CA2818304351
Gene: IL17RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085073C>G , CM000684.2:g.17085073C>G GRCh38
NC_000022.10:g.17565963C>G , CM000684.1:g.17565963C>G GRCh37
NC_000022.9:g.15945963C>G NCBI36
NG_028257.1:g.5113C>G , LRG_355:g.5113C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000694948.1:n.80C>G
ENST00000694949.1:n.77C>G
ENST00000694950.1:c.62C>G
ENST00000319363.11:c.-19C>G MANE Select ENSP00000320936.6:n.-19C>G
ENST00000319363.10:c.-19C>G ENSP00000320936.6:n.-19C>G
ENST00000459971.1:n.17C>G
ENST00000477874.1:n.120C>G
ENST00000612619.1:c.-19C>G ENSP00000479970.1:n.-19C>G
NM_001289905.1:c.-19C>G NP_001276834.1:n.-19C>G
NM_014339.6:c.-19C>G , LRG_355t1:c.-19C>G NP_055154.3:n.-19C>G
NM_014339.7:c.-19C>G MANE Select NP_055154.3:n.-19C>G
NM_001289905.2:c.-19C>G NP_001276834.1:n.-19C>G