Canonical Allele Identifier: CA2655109932

Gene: IL17RA

Linked Data

• gnomAD v4: 22-17085113-C-CCGT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085115_17085117dup , CM000684.2:g.17085115_17085117dup	GRCh38
NC_000022.10:g.17566005_17566007dup , CM000684.1:g.17566005_17566007dup	GRCh37
NC_000022.9:g.15946005_15946007dup	NCBI36
NG_028257.1:g.5155_5157dup , LRG_355:g.5155_5157dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.24_26dup	ENSP00000479970.1:p.Ser9_Ala10insSer
ENST00000694948.1:n.122_124dup
ENST00000694949.1:n.119_121dup
ENST00000694950.1:c.104_106dup
ENST00000319363.11:c.24_26dup MANE Select	ENSP00000320936.6:p.Ser9_Ala10insSer
ENST00000319363.10:c.24_26dup	ENSP00000320936.6:p.Ser9_Ala10insSer
ENST00000459971.1:n.59_61dup
ENST00000477874.1:n.162_164dup
ENST00000612619.1:c.24_26dup	ENSP00000479970.1:p.Ser9_Ala10insSer
NM_001289905.1:c.24_26dup	NP_001276834.1:p.Ser9_Ala10insSer
NM_014339.6:c.24_26dup , LRG_355t1:c.24_26dup	NP_055154.3:p.Ser9_Ala10insSer
NM_014339.7:c.24_26dup MANE Select	NP_055154.3:p.Ser9_Ala10insSer
NM_001289905.2:c.24_26dup	NP_001276834.1:p.Ser9_Ala10insSer