Canonical Allele Identifier: CA2655110044

Gene: IL17RA

Linked Data

• gnomAD v4: 22-17085296-C-CCGGACGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085300_17085307dup , CM000684.2:g.17085300_17085307dup	GRCh38
NC_000022.10:g.17566190_17566197dup , CM000684.1:g.17566190_17566197dup	GRCh37
NC_000022.9:g.15946190_15946197dup	NCBI36
NG_028257.1:g.5340_5347dup , LRG_355:g.5340_5347dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+71_138+78dup	ENSP00000479970.1:n.138+71_138+78dup
ENST00000694948.1:n.236+71_236+78dup
ENST00000694949.1:n.233+71_233+78dup
ENST00000694950.1:c.218+71_218+78dup
ENST00000319363.11:c.138+71_138+78dup MANE Select	ENSP00000320936.6:n.138+71_138+78dup
ENST00000319363.10:c.138+71_138+78dup	ENSP00000320936.6:n.138+71_138+78dup
ENST00000459971.1:n.173+71_173+78dup
ENST00000477874.1:n.276+71_276+78dup
ENST00000612619.1:c.138+71_138+78dup	ENSP00000479970.1:n.138+71_138+78dup
NM_001289905.1:c.138+71_138+78dup	NP_001276834.1:n.138+71_138+78dup
NM_014339.6:c.138+71_138+78dup , LRG_355t1:c.138+71_138+78dup	NP_055154.3:n.138+71_138+78dup
NM_014339.7:c.138+71_138+78dup MANE Select	NP_055154.3:n.138+71_138+78dup
NM_001289905.2:c.138+71_138+78dup	NP_001276834.1:n.138+71_138+78dup