Canonical Allele Identifier: CA10086203

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 340561
• ClinVar RCV Id: RCV000293416 ; RCV000454833 ; RCV001730672
• dbSNP Id: rs917865
• ExAC: 22:17565974 G / C
• gnomAD v2: 22-17565974-G-C
• gnomAD v3: 22-17085084-G-C
• gnomAD v4: 22-17085084-G-C
• MyVariant Identifiers: chr22:g.17565974G>C (hg19) ; chr22:g.17085084G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085084G>C , CM000684.2:g.17085084G>C	GRCh38
NC_000022.10:g.17565974G>C , CM000684.1:g.17565974G>C	GRCh37
NC_000022.9:g.15945974G>C	NCBI36
NG_028257.1:g.5124G>C , LRG_355:g.5124G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000694948.1:n.91G>C
ENST00000694949.1:n.88G>C
ENST00000694950.1:c.73G>C
ENST00000319363.11:c.-8G>C MANE Select	ENSP00000320936.6:n.-8G>C
ENST00000319363.10:c.-8G>C	ENSP00000320936.6:n.-8G>C
ENST00000459971.1:n.28G>C
ENST00000477874.1:n.131G>C
ENST00000612619.1:c.-8G>C	ENSP00000479970.1:n.-8G>C
NM_001289905.1:c.-8G>C	NP_001276834.1:n.-8G>C
NM_014339.6:c.-8G>C , LRG_355t1:c.-8G>C	NP_055154.3:n.-8G>C
NM_014339.7:c.-8G>C MANE Select	NP_055154.3:n.-8G>C
NM_001289905.2:c.-8G>C	NP_001276834.1:n.-8G>C