Canonical Allele Identifier: CA2577636841

Gene: IL17RA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085286_17085294del , CM000684.2:g.17085286_17085294del	GRCh38
NC_000022.10:g.17566176_17566184del , CM000684.1:g.17566176_17566184del	GRCh37
NC_000022.9:g.15946176_15946184del	NCBI36
NG_028257.1:g.5326_5334del , LRG_355:g.5326_5334del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+57_138+65del	ENSP00000479970.1:n.138+57_138+65del
ENST00000694948.1:n.236+57_236+65del
ENST00000694949.1:n.233+57_233+65del
ENST00000694950.1:c.218+57_218+65del
ENST00000319363.11:c.138+57_138+65del MANE Select	ENSP00000320936.6:n.138+57_138+65del
ENST00000319363.10:c.138+57_138+65del	ENSP00000320936.6:n.138+57_138+65del
ENST00000459971.1:n.173+57_173+65del
ENST00000477874.1:n.276+57_276+65del
ENST00000612619.1:c.138+57_138+65del	ENSP00000479970.1:n.138+57_138+65del
NM_001289905.1:c.138+57_138+65del	NP_001276834.1:n.138+57_138+65del
NM_014339.6:c.138+57_138+65del , LRG_355t1:c.138+57_138+65del	NP_055154.3:n.138+57_138+65del
NM_014339.7:c.138+57_138+65del MANE Select	NP_055154.3:n.138+57_138+65del
NM_001289905.2:c.138+57_138+65del	NP_001276834.1:n.138+57_138+65del