Canonical Allele Identifier: CA2655110034
Gene: IL17RA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17085292del , CM000684.2:g.17085292del GRCh38
NC_000022.10:g.17566182del , CM000684.1:g.17566182del GRCh37
NC_000022.9:g.15946182del NCBI36
NG_028257.1:g.5332del , LRG_355:g.5332del

Transcript Alleles

HGVS Amino-acid Change
ENST00000612619.2:c.138+63del ENSP00000479970.1:n.138+63del
ENST00000694948.1:n.236+63del
ENST00000694949.1:n.233+63del
ENST00000694950.1:c.218+63del
ENST00000319363.11:c.138+63del MANE Select ENSP00000320936.6:n.138+63del
ENST00000319363.10:c.138+63del ENSP00000320936.6:n.138+63del
ENST00000459971.1:n.173+63del
ENST00000477874.1:n.276+63del
ENST00000612619.1:c.138+63del ENSP00000479970.1:n.138+63del
NM_001289905.1:c.138+63del NP_001276834.1:n.138+63del
NM_014339.6:c.138+63del , LRG_355t1:c.138+63del NP_055154.3:n.138+63del
NM_014339.7:c.138+63del MANE Select NP_055154.3:n.138+63del
NM_001289905.2:c.138+63del NP_001276834.1:n.138+63del