Canonical Allele Identifier: CA638274638

Gene: IL17RA

Linked Data

• dbSNP Id: rs1172016907
• gnomAD v2: 22-17566042-CT-C
• gnomAD v3: 22-17085152-CT-C
• gnomAD v4: 22-17085152-CT-C
• MyVariant Identifiers: chr22:g.17566043del (hg19) ; chr22:g.17085153del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085153del , CM000684.2:g.17085153del	GRCh38
NC_000022.10:g.17566043del , CM000684.1:g.17566043del	GRCh37
NC_000022.9:g.15946043del	NCBI36
NG_028257.1:g.5193del , LRG_355:g.5193del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.62del	ENSP00000479970.1:p.Leu21ArgfsTer28
ENST00000694948.1:n.160del
ENST00000694949.1:n.157del
ENST00000694950.1:c.142del
ENST00000319363.11:c.62del MANE Select	ENSP00000320936.6:p.Leu21ArgfsTer28
ENST00000319363.10:c.62del	ENSP00000320936.6:p.Leu21ArgfsTer28
ENST00000459971.1:n.97del
ENST00000477874.1:n.200del
ENST00000612619.1:c.62del	ENSP00000479970.1:p.Leu21ArgfsTer28
NM_001289905.1:c.62del	NP_001276834.1:p.Leu21ArgfsTer28
NM_014339.6:c.62del , LRG_355t1:c.62del	NP_055154.3:p.Leu21ArgfsTer28
NM_014339.7:c.62del MANE Select	NP_055154.3:p.Leu21ArgfsTer28
NM_001289905.2:c.62del	NP_001276834.1:p.Leu21ArgfsTer28