Canonical Allele Identifier: CA2577636838
Gene: IL17RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085254A>C , CM000684.2:g.17085254A>C GRCh38
NC_000022.10:g.17566144A>C , CM000684.1:g.17566144A>C GRCh37
NC_000022.9:g.15946144A>C NCBI36
NG_028257.1:g.5294A>C , LRG_355:g.5294A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000612619.2:c.138+25A>C ENSP00000479970.1:n.138+25A>C
ENST00000694948.1:n.236+25A>C
ENST00000694949.1:n.233+25A>C
ENST00000694950.1:c.218+25A>C
ENST00000319363.11:c.138+25A>C MANE Select ENSP00000320936.6:n.138+25A>C
ENST00000319363.10:c.138+25A>C ENSP00000320936.6:n.138+25A>C
ENST00000459971.1:n.173+25A>C
ENST00000477874.1:n.276+25A>C
ENST00000612619.1:c.138+25A>C ENSP00000479970.1:n.138+25A>C
NM_001289905.1:c.138+25A>C NP_001276834.1:n.138+25A>C
NM_014339.6:c.138+25A>C , LRG_355t1:c.138+25A>C NP_055154.3:n.138+25A>C
NM_014339.7:c.138+25A>C MANE Select NP_055154.3:n.138+25A>C
NM_001289905.2:c.138+25A>C NP_001276834.1:n.138+25A>C