Canonical Allele Identifier: CA2751463729
Gene: IL1R2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.101994265del , CM000664.2:g.101994265del GRCh38
NC_000002.11:g.102610727del , CM000664.1:g.102610727del GRCh37
NC_000002.10:g.101977159del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000332549.8:c.-62+2254del MANE Select ENSP00000330959.3:n.-62+2254del
ENST00000332549.7:c.-62+2254del ENSP00000330959.3:n.-62+2254del
ENST00000464994.5:n.74+2232del
ENST00000493749.1:n.52+2254del
NM_001261419.1:c.-62+2254del NP_001248348.1:n.-62+2254del
NM_004633.3:c.-62+2254del NP_004624.1:n.-62+2254del
XM_006712734.2:c.-62+2269del XP_006712797.1:n.-62+2269del
XM_006712736.2:c.14+2232del XP_006712799.1:n.14+2232del
XM_006712734.3:c.-62+2269del XP_006712797.1:n.-62+2269del
XM_006712736.3:c.14+2232del XP_006712799.1:n.14+2232del
XM_017004889.1:c.-189+2254del XP_016860378.1:n.-189+2254del
XM_024453129.1:c.-157+2269del XP_024308897.1:n.-157+2269del
NM_004633.4:c.-62+2254del MANE Select NP_004624.1:n.-62+2254del
NM_001261419.2:c.-62+2254del NP_001248348.1:n.-62+2254del