Canonical Allele Identifier: CA410210271

Gene: IL17RA

Linked Data

• dbSNP Id: rs1226991818
• gnomAD v2: 22-17566097-G-T
• gnomAD v4: 22-17085207-G-T
• MyVariant Identifiers: chr22:g.17566097G>T (hg19) ; chr22:g.17085207G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085207G>T , CM000684.2:g.17085207G>T	GRCh38
NC_000022.10:g.17566097G>T , CM000684.1:g.17566097G>T	GRCh37
NC_000022.9:g.15946097G>T	NCBI36
NG_028257.1:g.5247G>T , LRG_355:g.5247G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.116G>T	ENSP00000479970.1:p.Arg39Leu
ENST00000694948.1:n.214G>T
ENST00000694949.1:n.211G>T
ENST00000694950.1:c.196G>T
ENST00000319363.11:c.116G>T MANE Select	ENSP00000320936.6:p.Arg39Leu
ENST00000319363.10:c.116G>T	ENSP00000320936.6:p.Arg39Leu
ENST00000459971.1:n.151G>T
ENST00000477874.1:n.254G>T
ENST00000612619.1:c.116G>T	ENSP00000479970.1:p.Arg39Leu
NM_001289905.1:c.116G>T	NP_001276834.1:p.Arg39Leu
NM_014339.6:c.116G>T , LRG_355t1:c.116G>T	NP_055154.3:p.Arg39Leu
NM_014339.7:c.116G>T MANE Select	NP_055154.3:p.Arg39Leu
NM_001289905.2:c.116G>T	NP_001276834.1:p.Arg39Leu