Canonical Allele Identifier: CA410210893

Gene: IL17RA

Linked Data

• dbSNP Id: rs2061373581
• MyVariant Identifiers: chr22:g.17578699A>G (hg19) ; chr22:g.17097809A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17097809A>G , CM000684.2:g.17097809A>G	GRCh38
NC_000022.10:g.17578699A>G , CM000684.1:g.17578699A>G	GRCh37
NC_000022.9:g.15958699A>G	NCBI36
NG_028257.1:g.17849A>G , LRG_355:g.17849A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000612619.2:c.176A>G	ENSP00000479970.1:p.Asp59Gly
ENST00000694948.1:n.274A>G
ENST00000694949.1:n.271A>G
ENST00000694950.1:c.244-47A>G
ENST00000694951.1:n.39A>G
ENST00000319363.11:c.176A>G MANE Select	ENSP00000320936.6:p.Asp59Gly
ENST00000319363.10:c.176A>G	ENSP00000320936.6:p.Asp59Gly
ENST00000477874.1:n.289A>G
ENST00000612619.1:c.176A>G	ENSP00000479970.1:p.Asp59Gly
NM_001289905.1:c.176A>G	NP_001276834.1:p.Asp59Gly
NM_014339.6:c.176A>G , LRG_355t1:c.176A>G	NP_055154.3:p.Asp59Gly
NM_014339.7:c.176A>G MANE Select	NP_055154.3:p.Asp59Gly
NM_001289905.2:c.176A>G	NP_001276834.1:p.Asp59Gly