Canonical Allele Identifier: CA1428894002
Gene: IL1RAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190636516_190636517delinsTC , CM000665.2:g.190636516_190636517delinsTC GRCh38
NC_000003.11:g.190354305_190354306delinsTC , CM000665.1:g.190354305_190354306delinsTC GRCh37
NC_000003.10:g.191836999_191837000delinsTC NCBI36
NG_029105.1:g.127466_127467delinsTC
NG_029105.2:g.127466_127467delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000317757.8:c.1051+7018_1051+7019delinsTC ENSP00000314807.3:n.1051+7018_1051+7019delinsTC
ENST00000439062.6:c.1051+7018_1051+7019delinsTC ENSP00000401132.1:n.1051+7018_1051+7019delinsTC
ENST00000447382.6:c.1051+7018_1051+7019delinsTC MANE Select ENSP00000390541.1:n.1051+7018_1051+7019delinsTC
ENST00000072516.7:c.1051+7018_1051+7019delinsTC ENSP00000072516.3:n.1051+7018_1051+7019delinsTC
ENST00000317757.7:c.1051+7018_1051+7019delinsTC ENSP00000314807.3:n.1051+7018_1051+7019delinsTC
ENST00000342550.6:c.903-7732_903-7731delinsTC ENSP00000345829.2:n.903-7732_903-7731delinsTC
ENST00000412504.6:c.1051+7018_1051+7019delinsTC ENSP00000412053.2:n.1051+7018_1051+7019delinsTC
ENST00000413869.5:c.903-7732_903-7731delinsTC ENSP00000416296.1:n.903-7732_903-7731delinsTC
ENST00000439062.5:c.1051+7018_1051+7019delinsTC ENSP00000401132.1:n.1051+7018_1051+7019delinsTC
ENST00000443369.6:c.1051+7018_1051+7019delinsTC ENSP00000408893.2:n.1051+7018_1051+7019delinsTC
ENST00000447382.5:c.1051+7018_1051+7019delinsTC ENSP00000390541.1:n.1051+7018_1051+7019delinsTC
NM_001167928.1:c.1051+7018_1051+7019delinsTC NP_001161400.1:n.1051+7018_1051+7019delinsTC
NM_001167929.1:c.1051+7018_1051+7019delinsTC NP_001161401.1:n.1051+7018_1051+7019delinsTC
NM_001167931.1:c.1051+7018_1051+7019delinsTC NP_001161403.1:n.1051+7018_1051+7019delinsTC
NM_002182.3:c.1051+7018_1051+7019delinsTC NP_002173.1:n.1051+7018_1051+7019delinsTC
XM_005247433.2:c.1051+7018_1051+7019delinsTC XP_005247490.1:n.1051+7018_1051+7019delinsTC
XM_005247434.3:c.469+7018_469+7019delinsTC XP_005247491.1:n.469+7018_469+7019delinsTC
XM_011512794.1:c.1051+7018_1051+7019delinsTC XP_011511096.1:n.1051+7018_1051+7019delinsTC
NM_001364879.1:c.1051+7018_1051+7019delinsTC NP_001351808.1:n.1051+7018_1051+7019delinsTC
NM_001364881.1:c.1051+7018_1051+7019delinsTC NP_001351810.1:n.1051+7018_1051+7019delinsTC
NR_157352.1:n.1126-7732_1126-7731delinsTC
NR_157353.1:n.1039-7732_1039-7731delinsTC
XM_017006348.2:c.469+7018_469+7019delinsTC XP_016861837.1:n.469+7018_469+7019delinsTC
NM_002182.4:c.1051+7018_1051+7019delinsTC MANE Select NP_002173.1:n.1051+7018_1051+7019delinsTC
NM_001167928.2:c.1051+7018_1051+7019delinsTC NP_001161400.1:n.1051+7018_1051+7019delinsTC
NM_001167929.2:c.1051+7018_1051+7019delinsTC NP_001161401.1:n.1051+7018_1051+7019delinsTC
NM_001167931.2:c.1051+7018_1051+7019delinsTC NP_001161403.1:n.1051+7018_1051+7019delinsTC
NM_001364881.2:c.1051+7018_1051+7019delinsTC NP_001351810.1:n.1051+7018_1051+7019delinsTC
NR_157352.2:n.1126-7732_1126-7731delinsTC
NR_157353.2:n.1039-7732_1039-7731delinsTC