Canonical Allele Identifier: CA410210071

Gene: IL17RA

Linked Data

• gnomAD v4: 22-17085099-C-A
• MyVariant Identifiers: chr22:g.17565989C>A (hg19) ; chr22:g.17085099C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085099C>A , CM000684.2:g.17085099C>A	GRCh38
NC_000022.10:g.17565989C>A , CM000684.1:g.17565989C>A	GRCh37
NC_000022.9:g.15945989C>A	NCBI36
NG_028257.1:g.5139C>A , LRG_355:g.5139C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.8C>A	ENSP00000479970.1:p.Ala3Asp
ENST00000694948.1:n.106C>A
ENST00000694949.1:n.103C>A
ENST00000694950.1:c.88C>A
ENST00000319363.11:c.8C>A MANE Select	ENSP00000320936.6:p.Ala3Asp
ENST00000319363.10:c.8C>A	ENSP00000320936.6:p.Ala3Asp
ENST00000459971.1:n.43C>A
ENST00000477874.1:n.146C>A
ENST00000612619.1:c.8C>A	ENSP00000479970.1:p.Ala3Asp
NM_001289905.1:c.8C>A	NP_001276834.1:p.Ala3Asp
NM_014339.6:c.8C>A , LRG_355t1:c.8C>A	NP_055154.3:p.Ala3Asp
NM_014339.7:c.8C>A MANE Select	NP_055154.3:p.Ala3Asp
NM_001289905.2:c.8C>A	NP_001276834.1:p.Ala3Asp