Canonical Allele Identifier: CA410210076

Gene: IL17RA

Linked Data

• dbSNP Id: rs1300159939
• gnomAD v2: 22-17565992-C-A
• gnomAD v4: 22-17085102-C-A
• MyVariant Identifiers: chr22:g.17565992C>A (hg19) ; chr22:g.17085102C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085102C>A , CM000684.2:g.17085102C>A	GRCh38
NC_000022.10:g.17565992C>A , CM000684.1:g.17565992C>A	GRCh37
NC_000022.9:g.15945992C>A	NCBI36
NG_028257.1:g.5142C>A , LRG_355:g.5142C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.11C>A	ENSP00000479970.1:p.Ala4Glu
ENST00000694948.1:n.109C>A
ENST00000694949.1:n.106C>A
ENST00000694950.1:c.91C>A
ENST00000319363.11:c.11C>A MANE Select	ENSP00000320936.6:p.Ala4Glu
ENST00000319363.10:c.11C>A	ENSP00000320936.6:p.Ala4Glu
ENST00000459971.1:n.46C>A
ENST00000477874.1:n.149C>A
ENST00000612619.1:c.11C>A	ENSP00000479970.1:p.Ala4Glu
NM_001289905.1:c.11C>A	NP_001276834.1:p.Ala4Glu
NM_014339.6:c.11C>A , LRG_355t1:c.11C>A	NP_055154.3:p.Ala4Glu
NM_014339.7:c.11C>A MANE Select	NP_055154.3:p.Ala4Glu
NM_001289905.2:c.11C>A	NP_001276834.1:p.Ala4Glu