Canonical Allele Identifier: CA638274649

Gene: IL17RA

Linked Data

• gnomAD v2: 22-17566060-GC-G
• gnomAD v4: 22-17085170-GC-G
• MyVariant Identifiers: chr22:g.17566061del (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.83del	ENSP00000479970.1:p.Pro28ArgfsTer21
ENST00000694948.1:n.181del
ENST00000694949.1:n.178del
ENST00000694950.1:c.163del
ENST00000319363.11:c.83del MANE Select	ENSP00000320936.6:p.Pro28ArgfsTer21
ENST00000319363.10:c.83del	ENSP00000320936.6:p.Pro28ArgfsTer21
ENST00000459971.1:n.118del
ENST00000477874.1:n.221del
ENST00000612619.1:c.83del	ENSP00000479970.1:p.Pro28ArgfsTer21
NM_001289905.1:c.83del	NP_001276834.1:p.Pro28ArgfsTer21
NM_014339.6:c.83del , LRG_355t1:c.83del	NP_055154.3:p.Pro28ArgfsTer21
NM_014339.7:c.83del MANE Select	NP_055154.3:p.Pro28ArgfsTer21
NM_001289905.2:c.83del	NP_001276834.1:p.Pro28ArgfsTer21