Canonical Allele Identifier: CA410210884

Gene: IL17RA

Linked Data

• MyVariant Identifiers: chr22:g.17578698G>A (hg19) ; chr22:g.17097808G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000612619.2:c.175G>A	ENSP00000479970.1:p.Asp59Asn
ENST00000694948.1:n.273G>A
ENST00000694949.1:n.270G>A
ENST00000694950.1:c.244-48G>A
ENST00000694951.1:n.38G>A
ENST00000319363.11:c.175G>A MANE Select	ENSP00000320936.6:p.Asp59Asn
ENST00000319363.10:c.175G>A	ENSP00000320936.6:p.Asp59Asn
ENST00000477874.1:n.288G>A
ENST00000612619.1:c.175G>A	ENSP00000479970.1:p.Asp59Asn
NM_001289905.1:c.175G>A	NP_001276834.1:p.Asp59Asn
NM_014339.6:c.175G>A , LRG_355t1:c.175G>A	NP_055154.3:p.Asp59Asn
NM_014339.7:c.175G>A MANE Select	NP_055154.3:p.Asp59Asn
NM_001289905.2:c.175G>A	NP_001276834.1:p.Asp59Asn