Canonical Allele Identifier: CA410210208

Gene: IL17RA

Linked Data

• ClinVar Variation Id: 2049952
• ClinVar RCV Id: RCV002914277
• dbSNP Id: rs1487756841
• gnomAD v2: 22-17566064-C-T
• gnomAD v3: 22-17085174-C-T
• gnomAD v4: 22-17085174-C-T
• MyVariant Identifiers: chr22:g.17566064C>T (hg19) ; chr22:g.17085174C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085174C>T , CM000684.2:g.17085174C>T	GRCh38
NC_000022.10:g.17566064C>T , CM000684.1:g.17566064C>T	GRCh37
NC_000022.9:g.15946064C>T	NCBI36
NG_028257.1:g.5214C>T , LRG_355:g.5214C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.83C>T	ENSP00000479970.1:p.Pro28Leu
ENST00000694948.1:n.181C>T
ENST00000694949.1:n.178C>T
ENST00000694950.1:c.163C>T
ENST00000319363.11:c.83C>T MANE Select	ENSP00000320936.6:p.Pro28Leu
ENST00000319363.10:c.83C>T	ENSP00000320936.6:p.Pro28Leu
ENST00000459971.1:n.118C>T
ENST00000477874.1:n.221C>T
ENST00000612619.1:c.83C>T	ENSP00000479970.1:p.Pro28Leu
NM_001289905.1:c.83C>T	NP_001276834.1:p.Pro28Leu
NM_014339.6:c.83C>T , LRG_355t1:c.83C>T	NP_055154.3:p.Pro28Leu
NM_014339.7:c.83C>T MANE Select	NP_055154.3:p.Pro28Leu
NM_001289905.2:c.83C>T	NP_001276834.1:p.Pro28Leu