Canonical Allele Identifier: CA515840658
Gene: IL1RAPL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.29935687A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29917570A>G , CM000685.2:g.29917570A>G GRCh38
NC_000023.10:g.29935687A>G , CM000685.1:g.29935687A>G GRCh37
NC_000023.9:g.29845608A>G NCBI36
NG_008292.1:g.1335007A>G
NG_008292.2:g.1335007A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.885A>G MANE Select ENSP00000368278.1:p.Glu295=
ENST00000302196.5:c.108A>G ENSP00000305200.5:p.Glu36=
ENST00000378993.5:c.885A>G ENSP00000368278.1:p.Glu295=
NM_014271.3:c.885A>G NP_055086.1:p.Glu295=
XM_005274441.1:c.885A>G XP_005274498.1:p.Glu295=
XM_011545445.1:c.885A>G XP_011543747.1:p.Glu295=
XM_017029240.1:c.885A>G XP_016884729.1:p.Glu295=
XM_017029241.1:c.507A>G XP_016884730.1:p.Glu169=
NM_014271.4:c.885A>G MANE Select NP_055086.1:p.Glu295=