Canonical Allele Identifier: CA410210301
Gene: IL17RA HGNC NCBI

Linked Data

dbSNP Id: rs1213537715

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085222C>G , CM000684.2:g.17085222C>G GRCh38
NC_000022.10:g.17566112C>G , CM000684.1:g.17566112C>G GRCh37
NC_000022.9:g.15946112C>G NCBI36
NG_028257.1:g.5262C>G , LRG_355:g.5262C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000612619.2:c.131C>G ENSP00000479970.1:p.Ser44Cys
ENST00000694948.1:n.229C>G
ENST00000694949.1:n.226C>G
ENST00000694950.1:c.211C>G
ENST00000319363.11:c.131C>G MANE Select ENSP00000320936.6:p.Ser44Cys
ENST00000319363.10:c.131C>G ENSP00000320936.6:p.Ser44Cys
ENST00000459971.1:n.166C>G
ENST00000477874.1:n.269C>G
ENST00000612619.1:c.131C>G ENSP00000479970.1:p.Ser44Cys
NM_001289905.1:c.131C>G NP_001276834.1:p.Ser44Cys
NM_014339.6:c.131C>G , LRG_355t1:c.131C>G NP_055154.3:p.Ser44Cys
NM_014339.7:c.131C>G MANE Select NP_055154.3:p.Ser44Cys
NM_001289905.2:c.131C>G NP_001276834.1:p.Ser44Cys