Canonical Allele Identifier: CA2655109933

Gene: IL17RA

Linked Data

• gnomAD v4: 22-17085117-C-CGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085117_17085118insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG , CM000684.2:g.17085117_17085118insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG	GRCh38
NC_000022.10:g.17566007_17566008insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG , CM000684.1:g.17566007_17566008insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG	GRCh37
NC_000022.9:g.15946007_15946008insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG	NCBI36
NG_028257.1:g.5157_5158insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG , LRG_355:g.5157_5158insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.26_27insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG	ENSP00000479970.1:p.Ala10Ter
ENST00000694948.1:n.124_125insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG
ENST00000694949.1:n.121_122insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG
ENST00000694950.1:c.106_107insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG
ENST00000319363.11:c.26_27insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG MANE Select	ENSP00000320936.6:p.Ala10Ter
ENST00000319363.10:c.26_27insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG	ENSP00000320936.6:p.Ala10Ter
ENST00000459971.1:n.61_62insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG
ENST00000477874.1:n.164_165insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG
ENST00000612619.1:c.26_27insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG	ENSP00000479970.1:p.Ala10Ter
NM_001289905.1:c.26_27insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG	NP_001276834.1:p.Ala10Ter
NM_014339.6:c.26_27insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG , LRG_355t1:c.26_27insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG	NP_055154.3:p.Ala10Ter
NM_014339.7:c.26_27insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG MANE Select	NP_055154.3:p.Ala10Ter
NM_001289905.2:c.26_27insGTGACTGGAGGCGGGAGTGACACCTCCGCCCGGGCCGCGGAGTTCGGGGAAGGAGGGCG	NP_001276834.1:p.Ala10Ter