Canonical Allele Identifier: CA412632725
Gene: IL1RAPL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.29417390T>A (hg19) chrX:g.29399273T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29399273T>A , CM000685.2:g.29399273T>A GRCh38
NC_000023.10:g.29417390T>A , CM000685.1:g.29417390T>A GRCh37
NC_000023.9:g.29327311T>A NCBI36
NG_008292.1:g.816710T>A
NG_008292.2:g.816710T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.668T>A MANE Select ENSP00000368278.1:p.Phe223Tyr
ENST00000378993.5:c.668T>A ENSP00000368278.1:p.Phe223Tyr
NM_014271.3:c.668T>A NP_055086.1:p.Phe223Tyr
XM_005274441.1:c.668T>A XP_005274498.1:p.Phe223Tyr
XM_011545445.1:c.668T>A XP_011543747.1:p.Phe223Tyr
XM_017029240.1:c.668T>A XP_016884729.1:p.Phe223Tyr
XM_017029241.1:c.290T>A XP_016884730.1:p.Phe97Tyr
NM_014271.4:c.668T>A MANE Select NP_055086.1:p.Phe223Tyr
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