Canonical Allele Identifier: CA2818304359

Gene: IL17RA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085313_17085319del , CM000684.2:g.17085313_17085319del	GRCh38
NC_000022.10:g.17566203_17566209del , CM000684.1:g.17566203_17566209del	GRCh37
NC_000022.9:g.15946203_15946209del	NCBI36
NG_028257.1:g.5353_5359del , LRG_355:g.5353_5359del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+84_138+90del	ENSP00000479970.1:n.138+84_138+90del
ENST00000694948.1:n.236+84_236+90del
ENST00000694949.1:n.233+84_233+90del
ENST00000694950.1:c.218+84_218+90del
ENST00000319363.11:c.138+84_138+90del MANE Select	ENSP00000320936.6:n.138+84_138+90del
ENST00000319363.10:c.138+84_138+90del	ENSP00000320936.6:n.138+84_138+90del
ENST00000459971.1:n.173+84_173+90del
ENST00000477874.1:n.276+84_276+90del
ENST00000612619.1:c.138+84_138+90del	ENSP00000479970.1:n.138+84_138+90del
NM_001289905.1:c.138+84_138+90del	NP_001276834.1:n.138+84_138+90del
NM_014339.6:c.138+84_138+90del , LRG_355t1:c.138+84_138+90del	NP_055154.3:n.138+84_138+90del
NM_014339.7:c.138+84_138+90del MANE Select	NP_055154.3:n.138+84_138+90del
NM_001289905.2:c.138+84_138+90del	NP_001276834.1:n.138+84_138+90del