Canonical Allele Identifier: CA410210261

Gene: IL17RA

Linked Data

• dbSNP Id: rs1321999394
• gnomAD v2: 22-17566093-C-G
• gnomAD v4: 22-17085203-C-G
• MyVariant Identifiers: chr22:g.17566093C>G (hg19) ; chr22:g.17085203C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085203C>G , CM000684.2:g.17085203C>G	GRCh38
NC_000022.10:g.17566093C>G , CM000684.1:g.17566093C>G	GRCh37
NC_000022.9:g.15946093C>G	NCBI36
NG_028257.1:g.5243C>G , LRG_355:g.5243C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.112C>G	ENSP00000479970.1:p.His38Asp
ENST00000694948.1:n.210C>G
ENST00000694949.1:n.207C>G
ENST00000694950.1:c.192C>G
ENST00000319363.11:c.112C>G MANE Select	ENSP00000320936.6:p.His38Asp
ENST00000319363.10:c.112C>G	ENSP00000320936.6:p.His38Asp
ENST00000459971.1:n.147C>G
ENST00000477874.1:n.250C>G
ENST00000612619.1:c.112C>G	ENSP00000479970.1:p.His38Asp
NM_001289905.1:c.112C>G	NP_001276834.1:p.His38Asp
NM_014339.6:c.112C>G , LRG_355t1:c.112C>G	NP_055154.3:p.His38Asp
NM_014339.7:c.112C>G MANE Select	NP_055154.3:p.His38Asp
NM_001289905.2:c.112C>G	NP_001276834.1:p.His38Asp