Canonical Allele Identifier: CA751263580

Gene: IL17RA

Linked Data

• dbSNP Id: rs1273011601
• MyVariant Identifiers: chr22:g.17566141_17566142del (hg19) ; chr22:g.17085251_17085252del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085251_17085252del , CM000684.2:g.17085251_17085252del	GRCh38
NC_000022.10:g.17566141_17566142del , CM000684.1:g.17566141_17566142del	GRCh37
NC_000022.9:g.15946141_15946142del	NCBI36
NG_028257.1:g.5291_5292del , LRG_355:g.5291_5292del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+22_138+23del	ENSP00000479970.1:n.138+22_138+23del
ENST00000694948.1:n.236+22_236+23del
ENST00000694949.1:n.233+22_233+23del
ENST00000694950.1:c.218+22_218+23del
ENST00000319363.11:c.138+22_138+23del MANE Select	ENSP00000320936.6:n.138+22_138+23del
ENST00000319363.10:c.138+22_138+23del	ENSP00000320936.6:n.138+22_138+23del
ENST00000459971.1:n.173+22_173+23del
ENST00000477874.1:n.276+22_276+23del
ENST00000612619.1:c.138+22_138+23del	ENSP00000479970.1:n.138+22_138+23del
NM_001289905.1:c.138+22_138+23del	NP_001276834.1:n.138+22_138+23del
NM_014339.6:c.138+22_138+23del , LRG_355t1:c.138+22_138+23del	NP_055154.3:n.138+22_138+23del
NM_014339.7:c.138+22_138+23del MANE Select	NP_055154.3:n.138+22_138+23del
NM_001289905.2:c.138+22_138+23del	NP_001276834.1:n.138+22_138+23del