Canonical Allele Identifier: CA512867438

Gene: IL17RA

Linked Data

• gnomAD v4: 22-17085178-T-G
• MyVariant Identifiers: chr22:g.17566068T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085178T>G , CM000684.2:g.17085178T>G	GRCh38
NC_000022.10:g.17566068T>G , CM000684.1:g.17566068T>G	GRCh37
NC_000022.9:g.15946068T>G	NCBI36
NG_028257.1:g.5218T>G , LRG_355:g.5218T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.87T>G	ENSP00000479970.1:p.Gly29=
ENST00000694948.1:n.185T>G
ENST00000694949.1:n.182T>G
ENST00000694950.1:c.167T>G
ENST00000319363.11:c.87T>G MANE Select	ENSP00000320936.6:p.Gly29=
ENST00000319363.10:c.87T>G	ENSP00000320936.6:p.Gly29=
ENST00000459971.1:n.122T>G
ENST00000477874.1:n.225T>G
ENST00000612619.1:c.87T>G	ENSP00000479970.1:p.Gly29=
NM_001289905.1:c.87T>G	NP_001276834.1:p.Gly29=
NM_014339.6:c.87T>G , LRG_355t1:c.87T>G	NP_055154.3:p.Gly29=
NM_014339.7:c.87T>G MANE Select	NP_055154.3:p.Gly29=
NM_001289905.2:c.87T>G	NP_001276834.1:p.Gly29=