Canonical Allele Identifier: CA2421802594
Gene: IL1RAPL1 HGNC NCBI

Linked Data

dbSNP Id: rs1924505546

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29622924_29622927del , CM000685.2:g.29622924_29622927del GRCh38
NC_000023.10:g.29641041_29641044del , CM000685.1:g.29641041_29641044del GRCh37
NC_000023.9:g.29550962_29550965del NCBI36
NG_008292.1:g.1040361_1040364del
NG_008292.2:g.1040361_1040364del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.704-45506_704-45503del MANE Select ENSP00000368278.1:n.704-45506_704-45503del
ENST00000378993.5:c.704-45506_704-45503del ENSP00000368278.1:n.704-45506_704-45503del
NM_014271.3:c.704-45506_704-45503del NP_055086.1:n.704-45506_704-45503del
XM_005274441.1:c.704-45506_704-45503del XP_005274498.1:n.704-45506_704-45503del
XM_011545445.1:c.704-45506_704-45503del XP_011543747.1:n.704-45506_704-45503del
XM_017029240.1:c.704-45506_704-45503del XP_016884729.1:n.704-45506_704-45503del
XM_017029241.1:c.326-45506_326-45503del XP_016884730.1:n.326-45506_326-45503del
NM_014271.4:c.704-45506_704-45503del MANE Select NP_055086.1:n.704-45506_704-45503del