Canonical Allele Identifier: CA2655110092

Gene: IL17RA

Linked Data

• gnomAD v4: 22-17085328-G-GTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085328_17085329insTGC , CM000684.2:g.17085328_17085329insTGC	GRCh38
NC_000022.10:g.17566218_17566219insTGC , CM000684.1:g.17566218_17566219insTGC	GRCh37
NC_000022.9:g.15946218_15946219insTGC	NCBI36
NG_028257.1:g.5368_5369insTGC , LRG_355:g.5368_5369insTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+99_138+100insTGC	ENSP00000479970.1:n.138+99_138+100insTGC
ENST00000694948.1:n.236+99_236+100insTGC
ENST00000694949.1:n.233+99_233+100insTGC
ENST00000694950.1:c.218+99_218+100insTGC
ENST00000319363.11:c.138+99_138+100insTGC MANE Select	ENSP00000320936.6:n.138+99_138+100insTGC
ENST00000319363.10:c.138+99_138+100insTGC	ENSP00000320936.6:n.138+99_138+100insTGC
ENST00000459971.1:n.173+99_173+100insTGC
ENST00000477874.1:n.276+99_276+100insTGC
ENST00000612619.1:c.138+99_138+100insTGC	ENSP00000479970.1:n.138+99_138+100insTGC
NM_001289905.1:c.138+99_138+100insTGC	NP_001276834.1:n.138+99_138+100insTGC
NM_014339.6:c.138+99_138+100insTGC , LRG_355t1:c.138+99_138+100insTGC	NP_055154.3:n.138+99_138+100insTGC
NM_014339.7:c.138+99_138+100insTGC MANE Select	NP_055154.3:n.138+99_138+100insTGC
NM_001289905.2:c.138+99_138+100insTGC	NP_001276834.1:n.138+99_138+100insTGC