Canonical Allele Identifier: CA638274707

Gene: IL17RA

Linked Data

• dbSNP Id: rs1444497670
• gnomAD v2: 22-17566195-C-CG
• gnomAD v3: 22-17085305-C-CG
• gnomAD v4: 22-17085305-C-CG
• MyVariant Identifiers: chr22:g.17566195_17566196insG (hg19) ; chr22:g.17085305_17085306insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085308dup , CM000684.2:g.17085308dup	GRCh38
NC_000022.10:g.17566198dup , CM000684.1:g.17566198dup	GRCh37
NC_000022.9:g.15946198dup	NCBI36
NG_028257.1:g.5348dup , LRG_355:g.5348dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+79dup	ENSP00000479970.1:n.138+79dup
ENST00000694948.1:n.236+79dup
ENST00000694949.1:n.233+79dup
ENST00000694950.1:c.218+79dup
ENST00000319363.11:c.138+79dup MANE Select	ENSP00000320936.6:n.138+79dup
ENST00000319363.10:c.138+79dup	ENSP00000320936.6:n.138+79dup
ENST00000459971.1:n.173+79dup
ENST00000477874.1:n.276+79dup
ENST00000612619.1:c.138+79dup	ENSP00000479970.1:n.138+79dup
NM_001289905.1:c.138+79dup	NP_001276834.1:n.138+79dup
NM_014339.6:c.138+79dup , LRG_355t1:c.138+79dup	NP_055154.3:n.138+79dup
NM_014339.7:c.138+79dup MANE Select	NP_055154.3:n.138+79dup
NM_001289905.2:c.138+79dup	NP_001276834.1:n.138+79dup