Canonical Allele Identifier: CA2655110109

Gene: IL17RA

Linked Data

• gnomAD v4: 22-17085337-AGTCCGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085339_17085344del , CM000684.2:g.17085339_17085344del	GRCh38
NC_000022.10:g.17566229_17566234del , CM000684.1:g.17566229_17566234del	GRCh37
NC_000022.9:g.15946229_15946234del	NCBI36
NG_028257.1:g.5379_5384del , LRG_355:g.5379_5384del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+110_138+115del	ENSP00000479970.1:n.138+110_138+115del
ENST00000694948.1:n.236+110_236+115del
ENST00000694949.1:n.233+110_233+115del
ENST00000694950.1:c.218+110_218+115del
ENST00000319363.11:c.138+110_138+115del MANE Select	ENSP00000320936.6:n.138+110_138+115del
ENST00000319363.10:c.138+110_138+115del	ENSP00000320936.6:n.138+110_138+115del
ENST00000459971.1:n.173+110_173+115del
ENST00000477874.1:n.276+110_276+115del
ENST00000612619.1:c.138+110_138+115del	ENSP00000479970.1:n.138+110_138+115del
NM_001289905.1:c.138+110_138+115del	NP_001276834.1:n.138+110_138+115del
NM_014339.6:c.138+110_138+115del , LRG_355t1:c.138+110_138+115del	NP_055154.3:n.138+110_138+115del
NM_014339.7:c.138+110_138+115del MANE Select	NP_055154.3:n.138+110_138+115del
NM_001289905.2:c.138+110_138+115del	NP_001276834.1:n.138+110_138+115del