Canonical Allele Identifier: CA410210282

Gene: IL17RA

Linked Data

• dbSNP Id: rs2061322077
• gnomAD v3: 22-17085213-T-C
• gnomAD v4: 22-17085213-T-C
• MyVariant Identifiers: chr22:g.17566103T>C (hg19) ; chr22:g.17085213T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085213T>C , CM000684.2:g.17085213T>C	GRCh38
NC_000022.10:g.17566103T>C , CM000684.1:g.17566103T>C	GRCh37
NC_000022.9:g.15946103T>C	NCBI36
NG_028257.1:g.5253T>C , LRG_355:g.5253T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.122T>C	ENSP00000479970.1:p.Leu41Pro
ENST00000694948.1:n.220T>C
ENST00000694949.1:n.217T>C
ENST00000694950.1:c.202T>C
ENST00000319363.11:c.122T>C MANE Select	ENSP00000320936.6:p.Leu41Pro
ENST00000319363.10:c.122T>C	ENSP00000320936.6:p.Leu41Pro
ENST00000459971.1:n.157T>C
ENST00000477874.1:n.260T>C
ENST00000612619.1:c.122T>C	ENSP00000479970.1:p.Leu41Pro
NM_001289905.1:c.122T>C	NP_001276834.1:p.Leu41Pro
NM_014339.6:c.122T>C , LRG_355t1:c.122T>C	NP_055154.3:p.Leu41Pro
NM_014339.7:c.122T>C MANE Select	NP_055154.3:p.Leu41Pro
NM_001289905.2:c.122T>C	NP_001276834.1:p.Leu41Pro