Canonical Allele Identifier: CA410210248

Gene: IL17RA

Linked Data

• gnomAD v4: 22-17085197-C-A
• MyVariant Identifiers: chr22:g.17566087C>A (hg19) ; chr22:g.17085197C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085197C>A , CM000684.2:g.17085197C>A	GRCh38
NC_000022.10:g.17566087C>A , CM000684.1:g.17566087C>A	GRCh37
NC_000022.9:g.15946087C>A	NCBI36
NG_028257.1:g.5237C>A , LRG_355:g.5237C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.106C>A	ENSP00000479970.1:p.Leu36Met
ENST00000694948.1:n.204C>A
ENST00000694949.1:n.201C>A
ENST00000694950.1:c.186C>A
ENST00000319363.11:c.106C>A MANE Select	ENSP00000320936.6:p.Leu36Met
ENST00000319363.10:c.106C>A	ENSP00000320936.6:p.Leu36Met
ENST00000459971.1:n.141C>A
ENST00000477874.1:n.244C>A
ENST00000612619.1:c.106C>A	ENSP00000479970.1:p.Leu36Met
NM_001289905.1:c.106C>A	NP_001276834.1:p.Leu36Met
NM_014339.6:c.106C>A , LRG_355t1:c.106C>A	NP_055154.3:p.Leu36Met
NM_014339.7:c.106C>A MANE Select	NP_055154.3:p.Leu36Met
NM_001289905.2:c.106C>A	NP_001276834.1:p.Leu36Met