Canonical Allele Identifier: CA2394917263
Gene: IL17RA HGNC NCBI

Linked Data

dbSNP Id: rs1218180010
gnomAD v4: 22-17085000-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085000G>A , CM000684.2:g.17085000G>A GRCh38
NC_000022.10:g.17565890G>A , CM000684.1:g.17565890G>A GRCh37
NC_000022.9:g.15945890G>A NCBI36
NG_028257.1:g.5040G>A , LRG_355:g.5040G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000694948.1:n.7G>A
ENST00000694949.1:n.4G>A
ENST00000319363.11:c.-92G>A MANE Select ENSP00000320936.6:n.-92G>A
ENST00000319363.10:c.-92G>A ENSP00000320936.6:n.-92G>A
ENST00000477874.1:n.47G>A
ENST00000612619.1:c.-92G>A ENSP00000479970.1:n.-92G>A
NM_001289905.1:c.-92G>A NP_001276834.1:n.-92G>A
NM_014339.6:c.-92G>A , LRG_355t1:c.-92G>A NP_055154.3:n.-92G>A
NM_014339.7:c.-92G>A MANE Select NP_055154.3:n.-92G>A
NM_001289905.2:c.-92G>A NP_001276834.1:n.-92G>A
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