Canonical Allele Identifier: CA10086210

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 1046681
• ClinVar RCV Id: RCV001351273
• dbSNP Id: rs751990928
• ExAC: 22:17566031 GGCTGCTCCT / G
• gnomAD v2: 22-17566031-GGCTGCTCCT-G
• gnomAD v4: 22-17085141-GGCTGCTCCT-G
• MyVariant Identifiers: chr22:g.17566032_17566040del (hg19) ; chr22:g.17085142_17085150del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085152_17085160del , CM000684.2:g.17085152_17085160del	GRCh38
NC_000022.10:g.17566042_17566050del , CM000684.1:g.17566042_17566050del	GRCh37
NC_000022.9:g.15946042_15946050del	NCBI36
NG_028257.1:g.5192_5200del , LRG_355:g.5192_5200del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.61_69del	ENSP00000479970.1:p.Leu21_Leu23del
ENST00000694948.1:n.159_167del
ENST00000694949.1:n.156_164del
ENST00000694950.1:c.141_149del
ENST00000319363.11:c.61_69del MANE Select	ENSP00000320936.6:p.Leu21_Leu23del
ENST00000319363.10:c.61_69del	ENSP00000320936.6:p.Leu21_Leu23del
ENST00000459971.1:n.96_104del
ENST00000477874.1:n.199_207del
ENST00000612619.1:c.61_69del	ENSP00000479970.1:p.Leu21_Leu23del
NM_001289905.1:c.61_69del	NP_001276834.1:p.Leu21_Leu23del
NM_014339.6:c.61_69del , LRG_355t1:c.61_69del	NP_055154.3:p.Leu21_Leu23del
NM_014339.7:c.61_69del MANE Select	NP_055154.3:p.Leu21_Leu23del
NM_001289905.2:c.61_69del	NP_001276834.1:p.Leu21_Leu23del