Canonical Allele Identifier: CA2466563307

Gene: IRAK1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154013289G= , CM000685.2:g.154013289G=	GRCh38
NC_000023.10:g.153278740G= , CM000685.1:g.153278740G=	GRCh37
NC_000023.9:g.152931934G=	NCBI36
NG_008387.1:g.11603C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467236.2:n.464C=
ENST00000699980.1:n.1228C=
ENST00000369980.8:c.1684C= MANE Select	ENSP00000358997.3:p.Gln562=
ENST00000369973.7:c.*627C=	ENSP00000358990.3:n.*627C=
ENST00000369974.6:c.1447C=	ENSP00000358991.2:p.Gln483=
ENST00000369980.7:c.1684C=	ENSP00000358997.3:p.Gln562=
ENST00000393687.6:c.1594C=	ENSP00000377291.2:p.Gln532=
ENST00000429936.6:c.1672C=	ENSP00000392662.2:p.Gln558=
ENST00000437278.5:c.375C=
ENST00000443220.1:c.929C=
ENST00000444230.5:c.529-2173C=	ENSP00000399974.1:n.529-2173C=
ENST00000444254.1:c.350C=
ENST00000455690.5:c.280-611C=	ENSP00000411809.1:n.280-611C=
ENST00000477274.1:n.616-2478C=
NM_001025242.1:c.1594C=	NP_001020413.1:p.Gln532=
NM_001025243.1:c.1447C=	NP_001020414.1:p.Gln483=
NM_001569.3:c.1684C=	NP_001560.2:p.Gln562=
XM_005274668.2:c.1672C=	XP_005274725.1:p.Gln558=
XM_011531158.1:c.1357C=	XP_011529460.1:p.Gln453=
XM_005274668.4:c.1672C=	XP_005274725.1:p.Gln558=
NM_001569.4:c.1684C= MANE Select	NP_001560.2:p.Gln562=
NM_001025242.2:c.1594C=	NP_001020413.1:p.Gln532=
NM_001025243.2:c.1447C=	NP_001020414.1:p.Gln483=