Canonical Allele Identifier: CA512867086

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 1083289
• ClinVar RCV Id: RCV001399919
• dbSNP Id: rs2123786594
• gnomAD v4: 22-17085124-C-A
• MyVariant Identifiers: chr22:g.17566014C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085124C>A , CM000684.2:g.17085124C>A	GRCh38
NC_000022.10:g.17566014C>A , CM000684.1:g.17566014C>A	GRCh37
NC_000022.9:g.15946014C>A	NCBI36
NG_028257.1:g.5164C>A , LRG_355:g.5164C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.33C>A	ENSP00000479970.1:p.Val11=
ENST00000694948.1:n.131C>A
ENST00000694949.1:n.128C>A
ENST00000694950.1:c.113C>A
ENST00000319363.11:c.33C>A MANE Select	ENSP00000320936.6:p.Val11=
ENST00000319363.10:c.33C>A	ENSP00000320936.6:p.Val11=
ENST00000459971.1:n.68C>A
ENST00000477874.1:n.171C>A
ENST00000612619.1:c.33C>A	ENSP00000479970.1:p.Val11=
NM_001289905.1:c.33C>A	NP_001276834.1:p.Val11=
NM_014339.6:c.33C>A , LRG_355t1:c.33C>A	NP_055154.3:p.Val11=
NM_014339.7:c.33C>A MANE Select	NP_055154.3:p.Val11=
NM_001289905.2:c.33C>A	NP_001276834.1:p.Val11=