Canonical Allele Identifier: CA2655109989

Gene: IL17RA

Linked Data

• gnomAD v4: 22-17085268-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085268T>C , CM000684.2:g.17085268T>C	GRCh38
NC_000022.10:g.17566158T>C , CM000684.1:g.17566158T>C	GRCh37
NC_000022.9:g.15946158T>C	NCBI36
NG_028257.1:g.5308T>C , LRG_355:g.5308T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.138+39T>C	ENSP00000479970.1:n.138+39T>C
ENST00000694948.1:n.236+39T>C
ENST00000694949.1:n.233+39T>C
ENST00000694950.1:c.218+39T>C
ENST00000319363.11:c.138+39T>C MANE Select	ENSP00000320936.6:n.138+39T>C
ENST00000319363.10:c.138+39T>C	ENSP00000320936.6:n.138+39T>C
ENST00000459971.1:n.173+39T>C
ENST00000477874.1:n.276+39T>C
ENST00000612619.1:c.138+39T>C	ENSP00000479970.1:n.138+39T>C
NM_001289905.1:c.138+39T>C	NP_001276834.1:n.138+39T>C
NM_014339.6:c.138+39T>C , LRG_355t1:c.138+39T>C	NP_055154.3:n.138+39T>C
NM_014339.7:c.138+39T>C MANE Select	NP_055154.3:n.138+39T>C
NM_001289905.2:c.138+39T>C	NP_001276834.1:n.138+39T>C