Canonical Allele Identifier: CA410210090

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 2549939
• ClinVar RCV Id: RCV004315761
• dbSNP Id: rs2061321130
• gnomAD v4: 22-17085108-G-C
• MyVariant Identifiers: chr22:g.17565998G>C (hg19) ; chr22:g.17085108G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085108G>C , CM000684.2:g.17085108G>C	GRCh38
NC_000022.10:g.17565998G>C , CM000684.1:g.17565998G>C	GRCh37
NC_000022.9:g.15945998G>C	NCBI36
NG_028257.1:g.5148G>C , LRG_355:g.5148G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.17G>C	ENSP00000479970.1:p.Ser6Thr
ENST00000694948.1:n.115G>C
ENST00000694949.1:n.112G>C
ENST00000694950.1:c.97G>C
ENST00000319363.11:c.17G>C MANE Select	ENSP00000320936.6:p.Ser6Thr
ENST00000319363.10:c.17G>C	ENSP00000320936.6:p.Ser6Thr
ENST00000459971.1:n.52G>C
ENST00000477874.1:n.155G>C
ENST00000612619.1:c.17G>C	ENSP00000479970.1:p.Ser6Thr
NM_001289905.1:c.17G>C	NP_001276834.1:p.Ser6Thr
NM_014339.6:c.17G>C , LRG_355t1:c.17G>C	NP_055154.3:p.Ser6Thr
NM_014339.7:c.17G>C MANE Select	NP_055154.3:p.Ser6Thr
NM_001289905.2:c.17G>C	NP_001276834.1:p.Ser6Thr