Canonical Allele Identifier: CA410210280

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 898008
• ClinVar RCV Id: RCV001141594
• dbSNP Id: rs1295037189
• gnomAD v2: 22-17566102-C-G
• gnomAD v4: 22-17085212-C-G
• MyVariant Identifiers: chr22:g.17566102C>G (hg19) ; chr22:g.17085212C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085212C>G , CM000684.2:g.17085212C>G	GRCh38
NC_000022.10:g.17566102C>G , CM000684.1:g.17566102C>G	GRCh37
NC_000022.9:g.15946102C>G	NCBI36
NG_028257.1:g.5252C>G , LRG_355:g.5252C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.121C>G	ENSP00000479970.1:p.Leu41Val
ENST00000694948.1:n.219C>G
ENST00000694949.1:n.216C>G
ENST00000694950.1:c.201C>G
ENST00000319363.11:c.121C>G MANE Select	ENSP00000320936.6:p.Leu41Val
ENST00000319363.10:c.121C>G	ENSP00000320936.6:p.Leu41Val
ENST00000459971.1:n.156C>G
ENST00000477874.1:n.259C>G
ENST00000612619.1:c.121C>G	ENSP00000479970.1:p.Leu41Val
NM_001289905.1:c.121C>G	NP_001276834.1:p.Leu41Val
NM_014339.6:c.121C>G , LRG_355t1:c.121C>G	NP_055154.3:p.Leu41Val
NM_014339.7:c.121C>G MANE Select	NP_055154.3:p.Leu41Val
NM_001289905.2:c.121C>G	NP_001276834.1:p.Leu41Val