Canonical Allele Identifier: CA751263591

Gene: IL17RA

Linked Data

• dbSNP Id: rs1327392577
• gnomAD v3: 22-17085254-AG-A
• gnomAD v4: 22-17085254-AG-A
• MyVariant Identifiers: chr22:g.17566145del (hg19) ; chr22:g.17085255del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085255del , CM000684.2:g.17085255del	GRCh38
NC_000022.10:g.17566145del , CM000684.1:g.17566145del	GRCh37
NC_000022.9:g.15946145del	NCBI36
NG_028257.1:g.5295del , LRG_355:g.5295del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+26del	ENSP00000479970.1:n.138+26del
ENST00000694948.1:n.236+26del
ENST00000694949.1:n.233+26del
ENST00000694950.1:c.218+26del
ENST00000319363.11:c.138+26del MANE Select	ENSP00000320936.6:n.138+26del
ENST00000319363.10:c.138+26del	ENSP00000320936.6:n.138+26del
ENST00000459971.1:n.173+26del
ENST00000477874.1:n.276+26del
ENST00000612619.1:c.138+26del	ENSP00000479970.1:n.138+26del
NM_001289905.1:c.138+26del	NP_001276834.1:n.138+26del
NM_014339.6:c.138+26del , LRG_355t1:c.138+26del	NP_055154.3:n.138+26del
NM_014339.7:c.138+26del MANE Select	NP_055154.3:n.138+26del
NM_001289905.2:c.138+26del	NP_001276834.1:n.138+26del