Canonical Allele Identifier: CA415140926
Gene: IRAK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154013390A>T , CM000685.2:g.154013390A>T GRCh38
NC_000023.10:g.153278841A>T , CM000685.1:g.153278841A>T GRCh37
NC_000023.9:g.152932035A>T NCBI36
NG_008387.1:g.11502T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000467236.2:n.363T>A
ENST00000699980.1:n.1127T>A
ENST00000369980.8:c.1583T>A MANE Select ENSP00000358997.3:p.Val528Glu
ENST00000369973.7:c.*526T>A ENSP00000358990.3:n.*526T>A
ENST00000369974.6:c.1346T>A ENSP00000358991.2:p.Val449Glu
ENST00000369980.7:c.1583T>A ENSP00000358997.3:p.Val528Glu
ENST00000393687.6:c.1540-47T>A ENSP00000377291.2:n.1540-47T>A
ENST00000429936.6:c.1618-47T>A ENSP00000392662.2:n.1618-47T>A
ENST00000437278.5:c.321-47T>A
ENST00000443220.1:c.828T>A
ENST00000444230.5:c.529-2274T>A ENSP00000399974.1:n.529-2274T>A
ENST00000444254.1:c.249T>A
ENST00000455690.5:c.279+652T>A ENSP00000411809.1:n.279+652T>A
ENST00000467236.1:n.380T>A
ENST00000477274.1:n.616-2579T>A
NM_001025242.1:c.1540-47T>A NP_001020413.1:n.1540-47T>A
NM_001025243.1:c.1346T>A NP_001020414.1:p.Val449Glu
NM_001569.3:c.1583T>A NP_001560.2:p.Val528Glu
XM_005274668.2:c.1618-47T>A XP_005274725.1:n.1618-47T>A
XM_011531158.1:c.1303-47T>A XP_011529460.1:n.1303-47T>A
XM_005274668.4:c.1618-47T>A XP_005274725.1:n.1618-47T>A
NM_001569.4:c.1583T>A MANE Select NP_001560.2:p.Val528Glu
NM_001025242.2:c.1540-47T>A NP_001020413.1:n.1540-47T>A
NM_001025243.2:c.1346T>A NP_001020414.1:p.Val449Glu