Canonical Allele Identifier: CA410211160

Gene: IL17RA

Linked Data

• dbSNP Id: rs1391459999
• gnomAD v2: 22-17578798-C-G
• gnomAD v4: 22-17097908-C-G
• MyVariant Identifiers: chr22:g.17578798C>G (hg19) ; chr22:g.17097908C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17097908C>G , CM000684.2:g.17097908C>G	GRCh38
NC_000022.10:g.17578798C>G , CM000684.1:g.17578798C>G	GRCh37
NC_000022.9:g.15958798C>G	NCBI36
NG_028257.1:g.17948C>G , LRG_355:g.17948C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000612619.2:c.275C>G	ENSP00000479970.1:p.Pro92Arg
ENST00000694948.1:n.373C>G
ENST00000694949.1:n.370C>G
ENST00000694950.1:c.296C>G
ENST00000694951.1:n.138C>G
ENST00000319363.11:c.275C>G MANE Select	ENSP00000320936.6:p.Pro92Arg
ENST00000319363.10:c.275C>G	ENSP00000320936.6:p.Pro92Arg
ENST00000477874.1:n.388C>G
ENST00000612619.1:c.275C>G	ENSP00000479970.1:p.Pro92Arg
NM_001289905.1:c.275C>G	NP_001276834.1:p.Pro92Arg
NM_014339.6:c.275C>G , LRG_355t1:c.275C>G	NP_055154.3:p.Pro92Arg
NM_014339.7:c.275C>G MANE Select	NP_055154.3:p.Pro92Arg
NM_001289905.2:c.275C>G	NP_001276834.1:p.Pro92Arg