Canonical Allele Identifier: CA10086217

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 340564
• ClinVar RCV Id: RCV000289706
• dbSNP Id: rs534287611
• ExAC: 22:17566131 C / T
• gnomAD v2: 22-17566131-C-T
• gnomAD v3: 22-17085241-C-T
• gnomAD v4: 22-17085241-C-T
• MyVariant Identifiers: chr22:g.17566131C>T (hg19) ; chr22:g.17085241C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085241C>T , CM000684.2:g.17085241C>T	GRCh38
NC_000022.10:g.17566131C>T , CM000684.1:g.17566131C>T	GRCh37
NC_000022.9:g.15946131C>T	NCBI36
NG_028257.1:g.5281C>T , LRG_355:g.5281C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+12C>T	ENSP00000479970.1:n.138+12C>T
ENST00000694948.1:n.236+12C>T
ENST00000694949.1:n.233+12C>T
ENST00000694950.1:c.218+12C>T
ENST00000319363.11:c.138+12C>T MANE Select	ENSP00000320936.6:n.138+12C>T
ENST00000319363.10:c.138+12C>T	ENSP00000320936.6:n.138+12C>T
ENST00000459971.1:n.173+12C>T
ENST00000477874.1:n.276+12C>T
ENST00000612619.1:c.138+12C>T	ENSP00000479970.1:n.138+12C>T
NM_001289905.1:c.138+12C>T	NP_001276834.1:n.138+12C>T
NM_014339.6:c.138+12C>T , LRG_355t1:c.138+12C>T	NP_055154.3:n.138+12C>T
NM_014339.7:c.138+12C>T MANE Select	NP_055154.3:n.138+12C>T
NM_001289905.2:c.138+12C>T	NP_001276834.1:n.138+12C>T