Canonical Allele Identifier: CA2655110004

Gene: IL17RA

Linked Data

• gnomAD v4: 22-17085276-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085276_17085277insT , CM000684.2:g.17085276_17085277insT	GRCh38
NC_000022.10:g.17566166_17566167insT , CM000684.1:g.17566166_17566167insT	GRCh37
NC_000022.9:g.15946166_15946167insT	NCBI36
NG_028257.1:g.5316_5317insT , LRG_355:g.5316_5317insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+47_138+48insT	ENSP00000479970.1:n.138+47_138+48insT
ENST00000694948.1:n.236+47_236+48insT
ENST00000694949.1:n.233+47_233+48insT
ENST00000694950.1:c.218+47_218+48insT
ENST00000319363.11:c.138+47_138+48insT MANE Select	ENSP00000320936.6:n.138+47_138+48insT
ENST00000319363.10:c.138+47_138+48insT	ENSP00000320936.6:n.138+47_138+48insT
ENST00000459971.1:n.173+47_173+48insT
ENST00000477874.1:n.276+47_276+48insT
ENST00000612619.1:c.138+47_138+48insT	ENSP00000479970.1:n.138+47_138+48insT
NM_001289905.1:c.138+47_138+48insT	NP_001276834.1:n.138+47_138+48insT
NM_014339.6:c.138+47_138+48insT , LRG_355t1:c.138+47_138+48insT	NP_055154.3:n.138+47_138+48insT
NM_014339.7:c.138+47_138+48insT MANE Select	NP_055154.3:n.138+47_138+48insT
NM_001289905.2:c.138+47_138+48insT	NP_001276834.1:n.138+47_138+48insT