Canonical Allele Identifier: CA410210129

Gene: IL17RA

Linked Data

• gnomAD v4: 22-17085129-G-C
• MyVariant Identifiers: chr22:g.17566019G>C (hg19) ; chr22:g.17085129G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17085129G>C , CM000684.2:g.17085129G>C	GRCh38
NC_000022.10:g.17566019G>C , CM000684.1:g.17566019G>C	GRCh37
NC_000022.9:g.15946019G>C	NCBI36
NG_028257.1:g.5169G>C , LRG_355:g.5169G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000612619.2:c.38G>C	ENSP00000479970.1:p.Gly13Ala
ENST00000694948.1:n.136G>C
ENST00000694949.1:n.133G>C
ENST00000694950.1:c.118G>C
ENST00000319363.11:c.38G>C MANE Select	ENSP00000320936.6:p.Gly13Ala
ENST00000319363.10:c.38G>C	ENSP00000320936.6:p.Gly13Ala
ENST00000459971.1:n.73G>C
ENST00000477874.1:n.176G>C
ENST00000612619.1:c.38G>C	ENSP00000479970.1:p.Gly13Ala
NM_001289905.1:c.38G>C	NP_001276834.1:p.Gly13Ala
NM_014339.6:c.38G>C , LRG_355t1:c.38G>C	NP_055154.3:p.Gly13Ala
NM_014339.7:c.38G>C MANE Select	NP_055154.3:p.Gly13Ala
NM_001289905.2:c.38G>C	NP_001276834.1:p.Gly13Ala