Canonical Allele Identifier: CA512867410

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 750206
• ClinVar RCV Id: RCV001392245
• dbSNP Id: rs1222771166
• gnomAD v2: 22-17566062-C-T
• gnomAD v3: 22-17085172-C-T
• gnomAD v4: 22-17085172-C-T
• MyVariant Identifiers: chr22:g.17566062C>T (hg19) ; chr22:g.17085172C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085172C>T , CM000684.2:g.17085172C>T	GRCh38
NC_000022.10:g.17566062C>T , CM000684.1:g.17566062C>T	GRCh37
NC_000022.9:g.15946062C>T	NCBI36
NG_028257.1:g.5212C>T , LRG_355:g.5212C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.81C>T	ENSP00000479970.1:p.Ala27=
ENST00000694948.1:n.179C>T
ENST00000694949.1:n.176C>T
ENST00000694950.1:c.161C>T
ENST00000319363.11:c.81C>T MANE Select	ENSP00000320936.6:p.Ala27=
ENST00000319363.10:c.81C>T	ENSP00000320936.6:p.Ala27=
ENST00000459971.1:n.116C>T
ENST00000477874.1:n.219C>T
ENST00000612619.1:c.81C>T	ENSP00000479970.1:p.Ala27=
NM_001289905.1:c.81C>T	NP_001276834.1:p.Ala27=
NM_014339.6:c.81C>T , LRG_355t1:c.81C>T	NP_055154.3:p.Ala27=
NM_014339.7:c.81C>T MANE Select	NP_055154.3:p.Ala27=
NM_001289905.2:c.81C>T	NP_001276834.1:p.Ala27=