Canonical Allele Identifier: CA2573157536

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 1568173
• ClinVar RCV Id: RCV002216849
• dbSNP Id: rs2123786856

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085237_17085238del , CM000684.2:g.17085237_17085238del	GRCh38
NC_000022.10:g.17566127_17566128del , CM000684.1:g.17566127_17566128del	GRCh37
NC_000022.9:g.15946127_15946128del	NCBI36
NG_028257.1:g.5277_5278del , LRG_355:g.5277_5278del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+8_138+9del	ENSP00000479970.1:n.138+8_138+9del
ENST00000694948.1:n.236+8_236+9del
ENST00000694949.1:n.233+8_233+9del
ENST00000694950.1:c.218+8_218+9del
ENST00000319363.11:c.138+8_138+9del MANE Select	ENSP00000320936.6:n.138+8_138+9del
ENST00000319363.10:c.138+8_138+9del	ENSP00000320936.6:n.138+8_138+9del
ENST00000459971.1:n.173+8_173+9del
ENST00000477874.1:n.276+8_276+9del
ENST00000612619.1:c.138+8_138+9del	ENSP00000479970.1:n.138+8_138+9del
NM_001289905.1:c.138+8_138+9del	NP_001276834.1:n.138+8_138+9del
NM_014339.6:c.138+8_138+9del , LRG_355t1:c.138+8_138+9del	NP_055154.3:n.138+8_138+9del
NM_014339.7:c.138+8_138+9del MANE Select	NP_055154.3:n.138+8_138+9del
NM_001289905.2:c.138+8_138+9del	NP_001276834.1:n.138+8_138+9del