Canonical Allele Identifier: CA321139661
Gene: IL17RA HGNC NCBI

Linked Data

dbSNP Id: rs1002099232
gnomAD v4: 22-17085008-C-A
MyVariant Identifiers: chr22:g.17565898C>A (hg19) chr22:g.17085008C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085008C>A , CM000684.2:g.17085008C>A GRCh38
NC_000022.10:g.17565898C>A , CM000684.1:g.17565898C>A GRCh37
NC_000022.9:g.15945898C>A NCBI36
NG_028257.1:g.5048C>A , LRG_355:g.5048C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000694948.1:n.15C>A
ENST00000694949.1:n.12C>A
ENST00000319363.11:c.-84C>A MANE Select ENSP00000320936.6:n.-84C>A
ENST00000319363.10:c.-84C>A ENSP00000320936.6:n.-84C>A
ENST00000477874.1:n.55C>A
ENST00000612619.1:c.-84C>A ENSP00000479970.1:n.-84C>A
NM_001289905.1:c.-84C>A NP_001276834.1:n.-84C>A
NM_014339.6:c.-84C>A , LRG_355t1:c.-84C>A NP_055154.3:n.-84C>A
NM_014339.7:c.-84C>A MANE Select NP_055154.3:n.-84C>A
NM_001289905.2:c.-84C>A NP_001276834.1:n.-84C>A
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