Canonical Allele Identifier: CA2693367463
Gene: IL1RAPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29917702_29917704del , CM000685.2:g.29917702_29917704del GRCh38
NC_000023.10:g.29935819_29935821del , CM000685.1:g.29935819_29935821del GRCh37
NC_000023.9:g.29845740_29845742del NCBI36
NG_008292.1:g.1335139_1335141del
NG_008292.2:g.1335139_1335141del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.911+106_911+108del MANE Select ENSP00000368278.1:n.911+106_911+108del
ENST00000302196.5:c.134+106_134+108del ENSP00000305200.5:n.134+106_134+108del
ENST00000378993.5:c.911+106_911+108del ENSP00000368278.1:n.911+106_911+108del
NM_014271.3:c.911+106_911+108del NP_055086.1:n.911+106_911+108del
XM_005274441.1:c.911+106_911+108del XP_005274498.1:n.911+106_911+108del
XM_011545445.1:c.911+106_911+108del XP_011543747.1:n.911+106_911+108del
XM_017029240.1:c.911+106_911+108del XP_016884729.1:n.911+106_911+108del
XM_017029241.1:c.533+106_533+108del XP_016884730.1:n.533+106_533+108del
NM_014271.4:c.911+106_911+108del MANE Select NP_055086.1:n.911+106_911+108del