Canonical Allele Identifier: CA512867657

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 1158315
• ClinVar RCV Id: RCV001501660
• dbSNP Id: rs1476573681
• gnomAD v4: 22-17085211-G-C
• MyVariant Identifiers: chr22:g.17566101G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085211G>C , CM000684.2:g.17085211G>C	GRCh38
NC_000022.10:g.17566101G>C , CM000684.1:g.17566101G>C	GRCh37
NC_000022.9:g.15946101G>C	NCBI36
NG_028257.1:g.5251G>C , LRG_355:g.5251G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.120G>C	ENSP00000479970.1:p.Ala40=
ENST00000694948.1:n.218G>C
ENST00000694949.1:n.215G>C
ENST00000694950.1:c.200G>C
ENST00000319363.11:c.120G>C MANE Select	ENSP00000320936.6:p.Ala40=
ENST00000319363.10:c.120G>C	ENSP00000320936.6:p.Ala40=
ENST00000459971.1:n.155G>C
ENST00000477874.1:n.258G>C
ENST00000612619.1:c.120G>C	ENSP00000479970.1:p.Ala40=
NM_001289905.1:c.120G>C	NP_001276834.1:p.Ala40=
NM_014339.6:c.120G>C , LRG_355t1:c.120G>C	NP_055154.3:p.Ala40=
NM_014339.7:c.120G>C MANE Select	NP_055154.3:p.Ala40=
NM_001289905.2:c.120G>C	NP_001276834.1:p.Ala40=