Canonical Allele Identifier: CA321139776
Gene: IL17RA HGNC NCBI

Linked Data

ClinVar Variation Id: 575944
ClinVar RCV Id: RCV000698300 RCV004026439
dbSNP Id: rs1006074686
gnomAD v2: 22-17566114-C-A
gnomAD v3: 22-17085224-C-A
gnomAD v4: 22-17085224-C-A
MyVariant Identifiers: chr22:g.17566114C>A (hg19) chr22:g.17085224C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085224C>A , CM000684.2:g.17085224C>A GRCh38
NC_000022.10:g.17566114C>A , CM000684.1:g.17566114C>A GRCh37
NC_000022.9:g.15946114C>A NCBI36
NG_028257.1:g.5264C>A , LRG_355:g.5264C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000612619.2:c.133C>A ENSP00000479970.1:p.Gln45Lys
ENST00000694948.1:n.231C>A
ENST00000694949.1:n.228C>A
ENST00000694950.1:c.213C>A
ENST00000319363.11:c.133C>A MANE Select ENSP00000320936.6:p.Gln45Lys
ENST00000319363.10:c.133C>A ENSP00000320936.6:p.Gln45Lys
ENST00000459971.1:n.168C>A
ENST00000477874.1:n.271C>A
ENST00000612619.1:c.133C>A ENSP00000479970.1:p.Gln45Lys
NM_001289905.1:c.133C>A NP_001276834.1:p.Gln45Lys
NM_014339.6:c.133C>A , LRG_355t1:c.133C>A NP_055154.3:p.Gln45Lys
NM_014339.7:c.133C>A MANE Select NP_055154.3:p.Gln45Lys
NM_001289905.2:c.133C>A NP_001276834.1:p.Gln45Lys
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