Canonical Allele Identifier: CA2818304356

Gene: IL17RA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085301_17085303del , CM000684.2:g.17085301_17085303del	GRCh38
NC_000022.10:g.17566191_17566193del , CM000684.1:g.17566191_17566193del	GRCh37
NC_000022.9:g.15946191_15946193del	NCBI36
NG_028257.1:g.5341_5343del , LRG_355:g.5341_5343del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+72_138+74del	ENSP00000479970.1:n.138+72_138+74del
ENST00000694948.1:n.236+72_236+74del
ENST00000694949.1:n.233+72_233+74del
ENST00000694950.1:c.218+72_218+74del
ENST00000319363.11:c.138+72_138+74del MANE Select	ENSP00000320936.6:n.138+72_138+74del
ENST00000319363.10:c.138+72_138+74del	ENSP00000320936.6:n.138+72_138+74del
ENST00000459971.1:n.173+72_173+74del
ENST00000477874.1:n.276+72_276+74del
ENST00000612619.1:c.138+72_138+74del	ENSP00000479970.1:n.138+72_138+74del
NM_001289905.1:c.138+72_138+74del	NP_001276834.1:n.138+72_138+74del
NM_014339.6:c.138+72_138+74del , LRG_355t1:c.138+72_138+74del	NP_055154.3:n.138+72_138+74del
NM_014339.7:c.138+72_138+74del MANE Select	NP_055154.3:n.138+72_138+74del
NM_001289905.2:c.138+72_138+74del	NP_001276834.1:n.138+72_138+74del