Canonical Allele Identifier: CA512866998

Gene: IL17RA

Linked Data

• gnomAD v4: 22-17085112-G-A
• MyVariant Identifiers: chr22:g.17566002G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085112G>A , CM000684.2:g.17085112G>A	GRCh38
NC_000022.10:g.17566002G>A , CM000684.1:g.17566002G>A	GRCh37
NC_000022.9:g.15946002G>A	NCBI36
NG_028257.1:g.5152G>A , LRG_355:g.5152G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.21G>A	ENSP00000479970.1:p.Pro7=
ENST00000694948.1:n.119G>A
ENST00000694949.1:n.116G>A
ENST00000694950.1:c.101G>A
ENST00000319363.11:c.21G>A MANE Select	ENSP00000320936.6:p.Pro7=
ENST00000319363.10:c.21G>A	ENSP00000320936.6:p.Pro7=
ENST00000459971.1:n.56G>A
ENST00000477874.1:n.159G>A
ENST00000612619.1:c.21G>A	ENSP00000479970.1:p.Pro7=
NM_001289905.1:c.21G>A	NP_001276834.1:p.Pro7=
NM_014339.6:c.21G>A , LRG_355t1:c.21G>A	NP_055154.3:p.Pro7=
NM_014339.7:c.21G>A MANE Select	NP_055154.3:p.Pro7=
NM_001289905.2:c.21G>A	NP_001276834.1:p.Pro7=