Canonical Allele Identifier: CA2579576852
Gene: IL1RAPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29917684_29917688del , CM000685.2:g.29917684_29917688del GRCh38
NC_000023.10:g.29935801_29935805del , CM000685.1:g.29935801_29935805del GRCh37
NC_000023.9:g.29845722_29845726del NCBI36
NG_008292.1:g.1335121_1335125del
NG_008292.2:g.1335121_1335125del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.911+88_911+92del MANE Select ENSP00000368278.1:n.911+88_911+92del
ENST00000302196.5:c.134+88_134+92del ENSP00000305200.5:n.134+88_134+92del
ENST00000378993.5:c.911+88_911+92del ENSP00000368278.1:n.911+88_911+92del
NM_014271.3:c.911+88_911+92del NP_055086.1:n.911+88_911+92del
XM_005274441.1:c.911+88_911+92del XP_005274498.1:n.911+88_911+92del
XM_011545445.1:c.911+88_911+92del XP_011543747.1:n.911+88_911+92del
XM_017029240.1:c.911+88_911+92del XP_016884729.1:n.911+88_911+92del
XM_017029241.1:c.533+88_533+92del XP_016884730.1:n.533+88_533+92del
NM_014271.4:c.911+88_911+92del MANE Select NP_055086.1:n.911+88_911+92del