Canonical Allele Identifier: CA2695094915
Gene: IRAK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154013395del , CM000685.2:g.154013395del GRCh38
NC_000023.10:g.153278846del , CM000685.1:g.153278846del GRCh37
NC_000023.9:g.152932040del NCBI36
NG_008387.1:g.11501del

Transcript Alleles

HGVS Amino-acid Change
ENST00000467236.2:n.362del
ENST00000699980.1:n.1126del
ENST00000369980.8:c.1582del MANE Select ENSP00000358997.3:p.Val528CysfsTer?
ENST00000369973.7:c.*525del ENSP00000358990.3:n.*525del
ENST00000369974.6:c.1345del ENSP00000358991.2:p.Val449CysfsTer?
ENST00000369980.7:c.1582del ENSP00000358997.3:p.Val528CysfsTer?
ENST00000393687.6:c.1540-48del ENSP00000377291.2:n.1540-48del
ENST00000429936.6:c.1618-48del ENSP00000392662.2:n.1618-48del
ENST00000437278.5:c.321-48del
ENST00000443220.1:c.827del
ENST00000444230.5:c.529-2275del ENSP00000399974.1:n.529-2275del
ENST00000444254.1:c.248del
ENST00000455690.5:c.279+651del ENSP00000411809.1:n.279+651del
ENST00000467236.1:n.379del
ENST00000477274.1:n.616-2580del
NM_001025242.1:c.1540-48del NP_001020413.1:n.1540-48del
NM_001025243.1:c.1345del NP_001020414.1:p.Val449CysfsTer?
NM_001569.3:c.1582del NP_001560.2:p.Val528CysfsTer?
XM_005274668.2:c.1618-48del XP_005274725.1:n.1618-48del
XM_011531158.1:c.1303-48del XP_011529460.1:n.1303-48del
XM_005274668.4:c.1618-48del XP_005274725.1:n.1618-48del
NM_001569.4:c.1582del MANE Select NP_001560.2:p.Val528CysfsTer?
NM_001025242.2:c.1540-48del NP_001020413.1:n.1540-48del
NM_001025243.2:c.1345del NP_001020414.1:p.Val449CysfsTer?