Canonical Allele Identifier: CA412635932
Gene: IL1RAPL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.29935667T>C (hg19) chrX:g.29917550T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29917550T>C , CM000685.2:g.29917550T>C GRCh38
NC_000023.10:g.29935667T>C , CM000685.1:g.29935667T>C GRCh37
NC_000023.9:g.29845588T>C NCBI36
NG_008292.1:g.1334987T>C
NG_008292.2:g.1334987T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.865T>C MANE Select ENSP00000368278.1:p.Phe289Leu
ENST00000302196.5:c.88T>C ENSP00000305200.5:p.Phe30Leu
ENST00000378993.5:c.865T>C ENSP00000368278.1:p.Phe289Leu
NM_014271.3:c.865T>C NP_055086.1:p.Phe289Leu
XM_005274441.1:c.865T>C XP_005274498.1:p.Phe289Leu
XM_011545445.1:c.865T>C XP_011543747.1:p.Phe289Leu
XM_017029240.1:c.865T>C XP_016884729.1:p.Phe289Leu
XM_017029241.1:c.487T>C XP_016884730.1:p.Phe163Leu
NM_014271.4:c.865T>C MANE Select NP_055086.1:p.Phe289Leu
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