Canonical Allele Identifier: CA2394917439

Gene: IL17RA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085243_17085244delinsTG , CM000684.2:g.17085243_17085244delinsTG	GRCh38
NC_000022.10:g.17566133_17566134delinsTG , CM000684.1:g.17566133_17566134delinsTG	GRCh37
NC_000022.9:g.15946133_15946134delinsTG	NCBI36
NG_028257.1:g.5283_5284delinsTG , LRG_355:g.5283_5284delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+14_138+15delinsTG	ENSP00000479970.1:n.138+14_138+15delinsTG
ENST00000694948.1:n.236+14_236+15delinsTG
ENST00000694949.1:n.233+14_233+15delinsTG
ENST00000694950.1:c.218+14_218+15delinsTG
ENST00000319363.11:c.138+14_138+15delinsTG MANE Select	ENSP00000320936.6:n.138+14_138+15delinsTG
ENST00000319363.10:c.138+14_138+15delinsTG	ENSP00000320936.6:n.138+14_138+15delinsTG
ENST00000459971.1:n.173+14_173+15delinsTG
ENST00000477874.1:n.276+14_276+15delinsTG
ENST00000612619.1:c.138+14_138+15delinsTG	ENSP00000479970.1:n.138+14_138+15delinsTG
NM_001289905.1:c.138+14_138+15delinsTG	NP_001276834.1:n.138+14_138+15delinsTG
NM_014339.6:c.138+14_138+15delinsTG , LRG_355t1:c.138+14_138+15delinsTG	NP_055154.3:n.138+14_138+15delinsTG
NM_014339.7:c.138+14_138+15delinsTG MANE Select	NP_055154.3:n.138+14_138+15delinsTG
NM_001289905.2:c.138+14_138+15delinsTG	NP_001276834.1:n.138+14_138+15delinsTG