Canonical Allele Identifier: CA2655109811
Gene: IL17RA HGNC NCBI

Linked Data

gnomAD v4: 22-17085007-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085007A>C , CM000684.2:g.17085007A>C GRCh38
NC_000022.10:g.17565897A>C , CM000684.1:g.17565897A>C GRCh37
NC_000022.9:g.15945897A>C NCBI36
NG_028257.1:g.5047A>C , LRG_355:g.5047A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000694948.1:n.14A>C
ENST00000694949.1:n.11A>C
ENST00000319363.11:c.-85A>C MANE Select ENSP00000320936.6:n.-85A>C
ENST00000319363.10:c.-85A>C ENSP00000320936.6:n.-85A>C
ENST00000477874.1:n.54A>C
ENST00000612619.1:c.-85A>C ENSP00000479970.1:n.-85A>C
NM_001289905.1:c.-85A>C NP_001276834.1:n.-85A>C
NM_014339.6:c.-85A>C , LRG_355t1:c.-85A>C NP_055154.3:n.-85A>C
NM_014339.7:c.-85A>C MANE Select NP_055154.3:n.-85A>C
NM_001289905.2:c.-85A>C NP_001276834.1:n.-85A>C
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