Canonical Allele Identifier: CA10086212

Gene: IL17RA

Linked Data

• dbSNP Id: rs757897521
• ExAC: 22:17566038 CCTG / C
• gnomAD v2: 22-17566038-CCTG-C
• gnomAD v4: 22-17085148-CCTG-C
• MyVariant Identifiers: chr22:g.17566039_17566041del (hg19) ; chr22:g.17085149_17085151del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085154_17085156del , CM000684.2:g.17085154_17085156del	GRCh38
NC_000022.10:g.17566044_17566046del , CM000684.1:g.17566044_17566046del	GRCh37
NC_000022.9:g.15946044_15946046del	NCBI36
NG_028257.1:g.5194_5196del , LRG_355:g.5194_5196del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.63_65del	ENSP00000479970.1:p.Leu22del
ENST00000694948.1:n.161_163del
ENST00000694949.1:n.158_160del
ENST00000694950.1:c.143_145del
ENST00000319363.11:c.63_65del MANE Select	ENSP00000320936.6:p.Leu22del
ENST00000319363.10:c.63_65del	ENSP00000320936.6:p.Leu22del
ENST00000459971.1:n.98_100del
ENST00000477874.1:n.201_203del
ENST00000612619.1:c.63_65del	ENSP00000479970.1:p.Leu22del
NM_001289905.1:c.63_65del	NP_001276834.1:p.Leu22del
NM_014339.6:c.63_65del , LRG_355t1:c.63_65del	NP_055154.3:p.Leu22del
NM_014339.7:c.63_65del MANE Select	NP_055154.3:p.Leu22del
NM_001289905.2:c.63_65del	NP_001276834.1:p.Leu22del