Canonical Allele Identifier: CA512867518

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 1146120
• ClinVar RCV Id: RCV001485270
• dbSNP Id: rs1387278734
• gnomAD v2: 22-17566081-C-A
• gnomAD v3: 22-17085191-C-A
• gnomAD v4: 22-17085191-C-A
• MyVariant Identifiers: chr22:g.17566081C>A (hg19) ; chr22:g.17085191C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085191C>A , CM000684.2:g.17085191C>A	GRCh38
NC_000022.10:g.17566081C>A , CM000684.1:g.17566081C>A	GRCh37
NC_000022.9:g.15946081C>A	NCBI36
NG_028257.1:g.5231C>A , LRG_355:g.5231C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.100C>A	ENSP00000479970.1:p.Arg34=
ENST00000694948.1:n.198C>A
ENST00000694949.1:n.195C>A
ENST00000694950.1:c.180C>A
ENST00000319363.11:c.100C>A MANE Select	ENSP00000320936.6:p.Arg34=
ENST00000319363.10:c.100C>A	ENSP00000320936.6:p.Arg34=
ENST00000459971.1:n.135C>A
ENST00000477874.1:n.238C>A
ENST00000612619.1:c.100C>A	ENSP00000479970.1:p.Arg34=
NM_001289905.1:c.100C>A	NP_001276834.1:p.Arg34=
NM_014339.6:c.100C>A , LRG_355t1:c.100C>A	NP_055154.3:p.Arg34=
NM_014339.7:c.100C>A MANE Select	NP_055154.3:p.Arg34=
NM_001289905.2:c.100C>A	NP_001276834.1:p.Arg34=