Canonical Allele Identifier: CA515840624
Gene: IL1RAPL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.29935615T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29917498T>C , CM000685.2:g.29917498T>C GRCh38
NC_000023.10:g.29935615T>C , CM000685.1:g.29935615T>C GRCh37
NC_000023.9:g.29845536T>C NCBI36
NG_008292.1:g.1334935T>C
NG_008292.2:g.1334935T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.813T>C MANE Select ENSP00000368278.1:p.Phe271=
ENST00000302196.5:c.36T>C ENSP00000305200.5:p.Phe12=
ENST00000378993.5:c.813T>C ENSP00000368278.1:p.Phe271=
NM_014271.3:c.813T>C NP_055086.1:p.Phe271=
XM_005274441.1:c.813T>C XP_005274498.1:p.Phe271=
XM_011545445.1:c.813T>C XP_011543747.1:p.Phe271=
XM_017029240.1:c.813T>C XP_016884729.1:p.Phe271=
XM_017029241.1:c.435T>C XP_016884730.1:p.Phe145=
NM_014271.4:c.813T>C MANE Select NP_055086.1:p.Phe271=