Canonical Allele Identifier: CA512869935

Gene: IL17RA

Linked Data

• MyVariant Identifiers: chr22:g.17578691C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17097801C>A , CM000684.2:g.17097801C>A	GRCh38
NC_000022.10:g.17578691C>A , CM000684.1:g.17578691C>A	GRCh37
NC_000022.9:g.15958691C>A	NCBI36
NG_028257.1:g.17841C>A , LRG_355:g.17841C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000612619.2:c.168C>A	ENSP00000479970.1:p.Thr56=
ENST00000694948.1:n.266C>A
ENST00000694949.1:n.263C>A
ENST00000694950.1:c.244-55C>A
ENST00000694951.1:n.31C>A
ENST00000319363.11:c.168C>A MANE Select	ENSP00000320936.6:p.Thr56=
ENST00000319363.10:c.168C>A	ENSP00000320936.6:p.Thr56=
ENST00000477874.1:n.281C>A
ENST00000612619.1:c.168C>A	ENSP00000479970.1:p.Thr56=
NM_001289905.1:c.168C>A	NP_001276834.1:p.Thr56=
NM_014339.6:c.168C>A , LRG_355t1:c.168C>A	NP_055154.3:p.Thr56=
NM_014339.7:c.168C>A MANE Select	NP_055154.3:p.Thr56=
NM_001289905.2:c.168C>A	NP_001276834.1:p.Thr56=