Canonical Allele Identifier: CA321139759

Gene: IL17RA

Linked Data

• dbSNP Id: rs993343144
• gnomAD v2: 22-17566063-C-A
• gnomAD v3: 22-17085173-C-A
• gnomAD v4: 22-17085173-C-A
• MyVariant Identifiers: chr22:g.17566063C>A (hg19) ; chr22:g.17085173C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085173C>A , CM000684.2:g.17085173C>A	GRCh38
NC_000022.10:g.17566063C>A , CM000684.1:g.17566063C>A	GRCh37
NC_000022.9:g.15946063C>A	NCBI36
NG_028257.1:g.5213C>A , LRG_355:g.5213C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.82C>A	ENSP00000479970.1:p.Pro28Thr
ENST00000694948.1:n.180C>A
ENST00000694949.1:n.177C>A
ENST00000694950.1:c.162C>A
ENST00000319363.11:c.82C>A MANE Select	ENSP00000320936.6:p.Pro28Thr
ENST00000319363.10:c.82C>A	ENSP00000320936.6:p.Pro28Thr
ENST00000459971.1:n.117C>A
ENST00000477874.1:n.220C>A
ENST00000612619.1:c.82C>A	ENSP00000479970.1:p.Pro28Thr
NM_001289905.1:c.82C>A	NP_001276834.1:p.Pro28Thr
NM_014339.6:c.82C>A , LRG_355t1:c.82C>A	NP_055154.3:p.Pro28Thr
NM_014339.7:c.82C>A MANE Select	NP_055154.3:p.Pro28Thr
NM_001289905.2:c.82C>A	NP_001276834.1:p.Pro28Thr