Canonical Allele Identifier: CA2466563346

Gene: IRAK1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154013412G= , CM000685.2:g.154013412G=	GRCh38
NC_000023.10:g.153278863G= , CM000685.1:g.153278863G=	GRCh37
NC_000023.9:g.152932057G=	NCBI36
NG_008387.1:g.11480C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467236.2:n.341C=
ENST00000699980.1:n.1105C=
ENST00000369980.8:c.1561C= MANE Select	ENSP00000358997.3:p.Leu521=
ENST00000369973.7:c.*504C=	ENSP00000358990.3:n.*504C=
ENST00000369974.6:c.1324C=	ENSP00000358991.2:p.Leu442=
ENST00000369980.7:c.1561C=	ENSP00000358997.3:p.Leu521=
ENST00000393687.6:c.1540-69C=	ENSP00000377291.2:n.1540-69C=
ENST00000429936.6:c.1618-69C=	ENSP00000392662.2:n.1618-69C=
ENST00000437278.5:c.321-69C=
ENST00000443220.1:c.806C=
ENST00000444230.5:c.529-2296C=	ENSP00000399974.1:n.529-2296C=
ENST00000444254.1:c.227C=
ENST00000455690.5:c.279+630C=	ENSP00000411809.1:n.279+630C=
ENST00000467236.1:n.358C=
ENST00000477274.1:n.616-2601C=
NM_001025242.1:c.1540-69C=	NP_001020413.1:n.1540-69C=
NM_001025243.1:c.1324C=	NP_001020414.1:p.Leu442=
NM_001569.3:c.1561C=	NP_001560.2:p.Leu521=
XM_005274668.2:c.1618-69C=	XP_005274725.1:n.1618-69C=
XM_011531158.1:c.1303-69C=	XP_011529460.1:n.1303-69C=
XM_005274668.4:c.1618-69C=	XP_005274725.1:n.1618-69C=
NM_001569.4:c.1561C= MANE Select	NP_001560.2:p.Leu521=
NM_001025242.2:c.1540-69C=	NP_001020413.1:n.1540-69C=
NM_001025243.2:c.1324C=	NP_001020414.1:p.Leu442=