Canonical Allele Identifier: CA14980093

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 2688175
• ClinVar RCV Id: RCV003489084
• dbSNP Id: rs2270242
• gnomAD v2: 22-17566229-T-A
• gnomAD v3: 22-17085339-T-A
• gnomAD v4: 22-17085339-T-A
• MyVariant Identifiers: chr22:g.17566229T>A (hg19) ; chr22:g.17085339T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085339T>A , CM000684.2:g.17085339T>A	GRCh38
NC_000022.10:g.17566229T>A , CM000684.1:g.17566229T>A	GRCh37
NC_000022.9:g.15946229T>A	NCBI36
NG_028257.1:g.5379T>A , LRG_355:g.5379T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+110T>A	ENSP00000479970.1:n.138+110T>A
ENST00000694948.1:n.236+110T>A
ENST00000694949.1:n.233+110T>A
ENST00000694950.1:c.218+110T>A
ENST00000319363.11:c.138+110T>A MANE Select	ENSP00000320936.6:n.138+110T>A
ENST00000319363.10:c.138+110T>A	ENSP00000320936.6:n.138+110T>A
ENST00000459971.1:n.173+110T>A
ENST00000477874.1:n.276+110T>A
ENST00000612619.1:c.138+110T>A	ENSP00000479970.1:n.138+110T>A
NM_001289905.1:c.138+110T>A	NP_001276834.1:n.138+110T>A
NM_014339.6:c.138+110T>A , LRG_355t1:c.138+110T>A	NP_055154.3:n.138+110T>A
NM_014339.7:c.138+110T>A MANE Select	NP_055154.3:n.138+110T>A
NM_001289905.2:c.138+110T>A	NP_001276834.1:n.138+110T>A