Canonical Allele Identifier: CA10086220

Gene: IL17RA

Linked Data

• dbSNP Id: rs781687086
• ExAC: 22:17566163 A / ACGCGGGGCAAGGT
• gnomAD v2: 22-17566163-A-ACGCGGGGCAAGGT
• gnomAD v3: 22-17085273-A-ACGCGGGGCAAGGT
• gnomAD v4: 22-17085273-A-ACGCGGGGCAAGGT
• MyVariant Identifiers: chr22:g.17566163_17566164insCGCGGGGCAAGGT (hg19) ; chr22:g.17085273_17085274insCGCGGGGCAAGGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085279_17085291dup , CM000684.2:g.17085279_17085291dup	GRCh38
NC_000022.10:g.17566169_17566181dup , CM000684.1:g.17566169_17566181dup	GRCh37
NC_000022.9:g.15946169_15946181dup	NCBI36
NG_028257.1:g.5319_5331dup , LRG_355:g.5319_5331dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+50_138+62dup	ENSP00000479970.1:n.138+50_138+62dup
ENST00000694948.1:n.236+50_236+62dup
ENST00000694949.1:n.233+50_233+62dup
ENST00000694950.1:c.218+50_218+62dup
ENST00000319363.11:c.138+50_138+62dup MANE Select	ENSP00000320936.6:n.138+50_138+62dup
ENST00000319363.10:c.138+50_138+62dup	ENSP00000320936.6:n.138+50_138+62dup
ENST00000459971.1:n.173+50_173+62dup
ENST00000477874.1:n.276+50_276+62dup
ENST00000612619.1:c.138+50_138+62dup	ENSP00000479970.1:n.138+50_138+62dup
NM_001289905.1:c.138+50_138+62dup	NP_001276834.1:n.138+50_138+62dup
NM_014339.6:c.138+50_138+62dup , LRG_355t1:c.138+50_138+62dup	NP_055154.3:n.138+50_138+62dup
NM_014339.7:c.138+50_138+62dup MANE Select	NP_055154.3:n.138+50_138+62dup
NM_001289905.2:c.138+50_138+62dup	NP_001276834.1:n.138+50_138+62dup