Canonical Allele Identifier: CA10086195

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 340557
• ClinVar RCV Id: RCV000372717 ; RCV003488559
• dbSNP Id: rs917864
• ExAC: 22:17565932 T / C
• gnomAD v2: 22-17565932-T-C
• gnomAD v3: 22-17085042-T-C
• gnomAD v4: 22-17085042-T-C
• MyVariant Identifiers: chr22:g.17565932T>C (hg19) ; chr22:g.17085042T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085042T>C , CM000684.2:g.17085042T>C	GRCh38
NC_000022.10:g.17565932T>C , CM000684.1:g.17565932T>C	GRCh37
NC_000022.9:g.15945932T>C	NCBI36
NG_028257.1:g.5082T>C , LRG_355:g.5082T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000694948.1:n.49T>C
ENST00000694949.1:n.46T>C
ENST00000694950.1:c.31T>C
ENST00000319363.11:c.-50T>C MANE Select	ENSP00000320936.6:n.-50T>C
ENST00000319363.10:c.-50T>C	ENSP00000320936.6:n.-50T>C
ENST00000477874.1:n.89T>C
ENST00000612619.1:c.-50T>C	ENSP00000479970.1:n.-50T>C
NM_001289905.1:c.-50T>C	NP_001276834.1:n.-50T>C
NM_014339.6:c.-50T>C , LRG_355t1:c.-50T>C	NP_055154.3:n.-50T>C
NM_014339.7:c.-50T>C MANE Select	NP_055154.3:n.-50T>C
NM_001289905.2:c.-50T>C	NP_001276834.1:n.-50T>C