Canonical Allele Identifier: CA321146384

Gene: IL17RA

Linked Data

• dbSNP Id: rs1055027140
• gnomAD v3: 22-17097730-C-T
• gnomAD v4: 22-17097730-C-T
• MyVariant Identifiers: chr22:g.17578620C>T (hg19) ; chr22:g.17097730C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17097730C>T , CM000684.2:g.17097730C>T	GRCh38
NC_000022.10:g.17578620C>T , CM000684.1:g.17578620C>T	GRCh37
NC_000022.9:g.15958620C>T	NCBI36
NG_028257.1:g.17770C>T , LRG_355:g.17770C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000612619.2:c.164-67C>T	ENSP00000479970.1:n.164-67C>T
ENST00000694948.1:n.262-67C>T
ENST00000694949.1:n.259-67C>T
ENST00000694950.1:c.244-126C>T
ENST00000694951.1:n.27-67C>T
ENST00000319363.11:c.164-67C>T MANE Select	ENSP00000320936.6:n.164-67C>T
ENST00000319363.10:c.164-67C>T	ENSP00000320936.6:n.164-67C>T
ENST00000477874.1:n.277-67C>T
ENST00000612619.1:c.164-67C>T	ENSP00000479970.1:n.164-67C>T
NM_001289905.1:c.164-67C>T	NP_001276834.1:n.164-67C>T
NM_014339.6:c.164-67C>T , LRG_355t1:c.164-67C>T	NP_055154.3:n.164-67C>T
NM_014339.7:c.164-67C>T MANE Select	NP_055154.3:n.164-67C>T
NM_001289905.2:c.164-67C>T	NP_001276834.1:n.164-67C>T