Canonical Allele Identifier: CA410210159

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 1524228
• ClinVar RCV Id: RCV002031566
• dbSNP Id: rs1429270259
• gnomAD v2: 22-17566036-C-T
• gnomAD v4: 22-17085146-C-T
• MyVariant Identifiers: chr22:g.17566036C>T (hg19) ; chr22:g.17085146C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085146C>T , CM000684.2:g.17085146C>T	GRCh38
NC_000022.10:g.17566036C>T , CM000684.1:g.17566036C>T	GRCh37
NC_000022.9:g.15946036C>T	NCBI36
NG_028257.1:g.5186C>T , LRG_355:g.5186C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.55C>T	ENSP00000479970.1:p.Leu19Phe
ENST00000694948.1:n.153C>T
ENST00000694949.1:n.150C>T
ENST00000694950.1:c.135C>T
ENST00000319363.11:c.55C>T MANE Select	ENSP00000320936.6:p.Leu19Phe
ENST00000319363.10:c.55C>T	ENSP00000320936.6:p.Leu19Phe
ENST00000459971.1:n.90C>T
ENST00000477874.1:n.193C>T
ENST00000612619.1:c.55C>T	ENSP00000479970.1:p.Leu19Phe
NM_001289905.1:c.55C>T	NP_001276834.1:p.Leu19Phe
NM_014339.6:c.55C>T , LRG_355t1:c.55C>T	NP_055154.3:p.Leu19Phe
NM_014339.7:c.55C>T MANE Select	NP_055154.3:p.Leu19Phe
NM_001289905.2:c.55C>T	NP_001276834.1:p.Leu19Phe