Canonical Allele Identifier: CA410210889

Gene: IL17RA

Linked Data

• dbSNP Id: rs1568918547
• MyVariant Identifiers: chr22:g.17578698G>T (hg19) ; chr22:g.17097808G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17097808G>T , CM000684.2:g.17097808G>T	GRCh38
NC_000022.10:g.17578698G>T , CM000684.1:g.17578698G>T	GRCh37
NC_000022.9:g.15958698G>T	NCBI36
NG_028257.1:g.17848G>T , LRG_355:g.17848G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000612619.2:c.175G>T	ENSP00000479970.1:p.Asp59Tyr
ENST00000694948.1:n.273G>T
ENST00000694949.1:n.270G>T
ENST00000694950.1:c.244-48G>T
ENST00000694951.1:n.38G>T
ENST00000319363.11:c.175G>T MANE Select	ENSP00000320936.6:p.Asp59Tyr
ENST00000319363.10:c.175G>T	ENSP00000320936.6:p.Asp59Tyr
ENST00000477874.1:n.288G>T
ENST00000612619.1:c.175G>T	ENSP00000479970.1:p.Asp59Tyr
NM_001289905.1:c.175G>T	NP_001276834.1:p.Asp59Tyr
NM_014339.6:c.175G>T , LRG_355t1:c.175G>T	NP_055154.3:p.Asp59Tyr
NM_014339.7:c.175G>T MANE Select	NP_055154.3:p.Asp59Tyr
NM_001289905.2:c.175G>T	NP_001276834.1:p.Asp59Tyr