Canonical Allele Identifier: CA2466563305

Gene: IRAK1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154013285G= , CM000685.2:g.154013285G=	GRCh38
NC_000023.10:g.153278736G= , CM000685.1:g.153278736G=	GRCh37
NC_000023.9:g.152931930G=	NCBI36
NG_008387.1:g.11607C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467236.2:n.468C=
ENST00000699980.1:n.1232C=
ENST00000369980.8:c.1688C= MANE Select	ENSP00000358997.3:p.Pro563=
ENST00000369973.7:c.*631C=	ENSP00000358990.3:n.*631C=
ENST00000369974.6:c.1451C=	ENSP00000358991.2:p.Pro484=
ENST00000369980.7:c.1688C=	ENSP00000358997.3:p.Pro563=
ENST00000393687.6:c.1598C=	ENSP00000377291.2:p.Pro533=
ENST00000429936.6:c.1676C=	ENSP00000392662.2:p.Pro559=
ENST00000437278.5:c.379C=
ENST00000443220.1:c.933C=
ENST00000444230.5:c.529-2169C=	ENSP00000399974.1:n.529-2169C=
ENST00000444254.1:c.354C=
ENST00000455690.5:c.280-607C=	ENSP00000411809.1:n.280-607C=
ENST00000477274.1:n.616-2474C=
NM_001025242.1:c.1598C=	NP_001020413.1:p.Pro533=
NM_001025243.1:c.1451C=	NP_001020414.1:p.Pro484=
NM_001569.3:c.1688C=	NP_001560.2:p.Pro563=
XM_005274668.2:c.1676C=	XP_005274725.1:p.Pro559=
XM_011531158.1:c.1361C=	XP_011529460.1:p.Pro454=
XM_005274668.4:c.1676C=	XP_005274725.1:p.Pro559=
NM_001569.4:c.1688C= MANE Select	NP_001560.2:p.Pro563=
NM_001025242.2:c.1598C=	NP_001020413.1:p.Pro533=
NM_001025243.2:c.1451C=	NP_001020414.1:p.Pro484=