Canonical Allele Identifier: CA410210089

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 2161151
• ClinVar RCV Id: RCV003087901
• gnomAD v4: 22-17085108-G-A
• MyVariant Identifiers: chr22:g.17565998G>A (hg19) ; chr22:g.17085108G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085108G>A , CM000684.2:g.17085108G>A	GRCh38
NC_000022.10:g.17565998G>A , CM000684.1:g.17565998G>A	GRCh37
NC_000022.9:g.15945998G>A	NCBI36
NG_028257.1:g.5148G>A , LRG_355:g.5148G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.17G>A	ENSP00000479970.1:p.Ser6Asn
ENST00000694948.1:n.115G>A
ENST00000694949.1:n.112G>A
ENST00000694950.1:c.97G>A
ENST00000319363.11:c.17G>A MANE Select	ENSP00000320936.6:p.Ser6Asn
ENST00000319363.10:c.17G>A	ENSP00000320936.6:p.Ser6Asn
ENST00000459971.1:n.52G>A
ENST00000477874.1:n.155G>A
ENST00000612619.1:c.17G>A	ENSP00000479970.1:p.Ser6Asn
NM_001289905.1:c.17G>A	NP_001276834.1:p.Ser6Asn
NM_014339.6:c.17G>A , LRG_355t1:c.17G>A	NP_055154.3:p.Ser6Asn
NM_014339.7:c.17G>A MANE Select	NP_055154.3:p.Ser6Asn
NM_001289905.2:c.17G>A	NP_001276834.1:p.Ser6Asn