Canonical Allele Identifier: CA512867227

Gene: IL17RA

Linked Data

• gnomAD v4: 22-17085145-G-T
• MyVariant Identifiers: chr22:g.17566035G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085145G>T , CM000684.2:g.17085145G>T	GRCh38
NC_000022.10:g.17566035G>T , CM000684.1:g.17566035G>T	GRCh37
NC_000022.9:g.15946035G>T	NCBI36
NG_028257.1:g.5185G>T , LRG_355:g.5185G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.54G>T	ENSP00000479970.1:p.Leu18=
ENST00000694948.1:n.152G>T
ENST00000694949.1:n.149G>T
ENST00000694950.1:c.134G>T
ENST00000319363.11:c.54G>T MANE Select	ENSP00000320936.6:p.Leu18=
ENST00000319363.10:c.54G>T	ENSP00000320936.6:p.Leu18=
ENST00000459971.1:n.89G>T
ENST00000477874.1:n.192G>T
ENST00000612619.1:c.54G>T	ENSP00000479970.1:p.Leu18=
NM_001289905.1:c.54G>T	NP_001276834.1:p.Leu18=
NM_014339.6:c.54G>T , LRG_355t1:c.54G>T	NP_055154.3:p.Leu18=
NM_014339.7:c.54G>T MANE Select	NP_055154.3:p.Leu18=
NM_001289905.2:c.54G>T	NP_001276834.1:p.Leu18=