Canonical Allele Identifier: CA2394917347
Gene: IL17RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085109C= , CM000684.2:g.17085109C= GRCh38
NC_000022.10:g.17565999C= , CM000684.1:g.17565999C= GRCh37
NC_000022.9:g.15945999C= NCBI36
NG_028257.1:g.5149C= , LRG_355:g.5149C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000612619.2:c.18C= ENSP00000479970.1:p.Ser6=
ENST00000694948.1:n.116C=
ENST00000694949.1:n.113C=
ENST00000694950.1:c.98C=
ENST00000319363.11:c.18C= MANE Select ENSP00000320936.6:p.Ser6=
ENST00000319363.10:c.18C= ENSP00000320936.6:p.Ser6=
ENST00000459971.1:n.53C=
ENST00000477874.1:n.156C=
ENST00000612619.1:c.18C= ENSP00000479970.1:p.Ser6=
NM_001289905.1:c.18C= NP_001276834.1:p.Ser6=
NM_014339.6:c.18C= , LRG_355t1:c.18C= NP_055154.3:p.Ser6=
NM_014339.7:c.18C= MANE Select NP_055154.3:p.Ser6=
NM_001289905.2:c.18C= NP_001276834.1:p.Ser6=