Canonical Allele Identifier: CA1428893956

Gene: IL1RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190636404_190636405delinsTG , CM000665.2:g.190636404_190636405delinsTG	GRCh38
NC_000003.11:g.190354193_190354194delinsTG , CM000665.1:g.190354193_190354194delinsTG	GRCh37
NC_000003.10:g.191836887_191836888delinsTG	NCBI36
NG_029105.1:g.127354_127355delinsTG
NG_029105.2:g.127354_127355delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317757.8:c.1051+6906_1051+6907delinsTG	ENSP00000314807.3:n.1051+6906_1051+6907delinsTG
ENST00000439062.6:c.1051+6906_1051+6907delinsTG	ENSP00000401132.1:n.1051+6906_1051+6907delinsTG
ENST00000447382.6:c.1051+6906_1051+6907delinsTG MANE Select	ENSP00000390541.1:n.1051+6906_1051+6907delinsTG
ENST00000072516.7:c.1051+6906_1051+6907delinsTG	ENSP00000072516.3:n.1051+6906_1051+6907delinsTG
ENST00000317757.7:c.1051+6906_1051+6907delinsTG	ENSP00000314807.3:n.1051+6906_1051+6907delinsTG
ENST00000342550.6:c.903-7844_903-7843delinsTG	ENSP00000345829.2:n.903-7844_903-7843delinsTG
ENST00000412504.6:c.1051+6906_1051+6907delinsTG	ENSP00000412053.2:n.1051+6906_1051+6907delinsTG
ENST00000413869.5:c.903-7844_903-7843delinsTG	ENSP00000416296.1:n.903-7844_903-7843delinsTG
ENST00000439062.5:c.1051+6906_1051+6907delinsTG	ENSP00000401132.1:n.1051+6906_1051+6907delinsTG
ENST00000443369.6:c.1051+6906_1051+6907delinsTG	ENSP00000408893.2:n.1051+6906_1051+6907delinsTG
ENST00000447382.5:c.1051+6906_1051+6907delinsTG	ENSP00000390541.1:n.1051+6906_1051+6907delinsTG
NM_001167928.1:c.1051+6906_1051+6907delinsTG	NP_001161400.1:n.1051+6906_1051+6907delinsTG
NM_001167929.1:c.1051+6906_1051+6907delinsTG	NP_001161401.1:n.1051+6906_1051+6907delinsTG
NM_001167931.1:c.1051+6906_1051+6907delinsTG	NP_001161403.1:n.1051+6906_1051+6907delinsTG
NM_002182.3:c.1051+6906_1051+6907delinsTG	NP_002173.1:n.1051+6906_1051+6907delinsTG
XM_005247433.2:c.1051+6906_1051+6907delinsTG	XP_005247490.1:n.1051+6906_1051+6907delinsTG
XM_005247434.3:c.469+6906_469+6907delinsTG	XP_005247491.1:n.469+6906_469+6907delinsTG
XM_011512794.1:c.1051+6906_1051+6907delinsTG	XP_011511096.1:n.1051+6906_1051+6907delinsTG
NM_001364879.1:c.1051+6906_1051+6907delinsTG	NP_001351808.1:n.1051+6906_1051+6907delinsTG
NM_001364881.1:c.1051+6906_1051+6907delinsTG	NP_001351810.1:n.1051+6906_1051+6907delinsTG
NR_157352.1:n.1126-7844_1126-7843delinsTG
NR_157353.1:n.1039-7844_1039-7843delinsTG
XM_017006348.2:c.469+6906_469+6907delinsTG	XP_016861837.1:n.469+6906_469+6907delinsTG
NM_002182.4:c.1051+6906_1051+6907delinsTG MANE Select	NP_002173.1:n.1051+6906_1051+6907delinsTG
NM_001167928.2:c.1051+6906_1051+6907delinsTG	NP_001161400.1:n.1051+6906_1051+6907delinsTG
NM_001167929.2:c.1051+6906_1051+6907delinsTG	NP_001161401.1:n.1051+6906_1051+6907delinsTG
NM_001167931.2:c.1051+6906_1051+6907delinsTG	NP_001161403.1:n.1051+6906_1051+6907delinsTG
NM_001364881.2:c.1051+6906_1051+6907delinsTG	NP_001351810.1:n.1051+6906_1051+6907delinsTG
NR_157352.2:n.1126-7844_1126-7843delinsTG
NR_157353.2:n.1039-7844_1039-7843delinsTG