Canonical Allele Identifier: CA2466563335

Gene: IRAK1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154013386G= , CM000685.2:g.154013386G=	GRCh38
NC_000023.10:g.153278837G= , CM000685.1:g.153278837G=	GRCh37
NC_000023.9:g.152932031G=	NCBI36
NG_008387.1:g.11506C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467236.2:n.367C=
ENST00000699980.1:n.1131C=
ENST00000369980.8:c.1587C= MANE Select	ENSP00000358997.3:p.Pro529=
ENST00000369973.7:c.*530C=	ENSP00000358990.3:n.*530C=
ENST00000369974.6:c.1350C=	ENSP00000358991.2:p.Pro450=
ENST00000369980.7:c.1587C=	ENSP00000358997.3:p.Pro529=
ENST00000393687.6:c.1540-43C=	ENSP00000377291.2:n.1540-43C=
ENST00000429936.6:c.1618-43C=	ENSP00000392662.2:n.1618-43C=
ENST00000437278.5:c.321-43C=
ENST00000443220.1:c.832C=
ENST00000444230.5:c.529-2270C=	ENSP00000399974.1:n.529-2270C=
ENST00000444254.1:c.253C=
ENST00000455690.5:c.279+656C=	ENSP00000411809.1:n.279+656C=
ENST00000467236.1:n.384C=
ENST00000477274.1:n.616-2575C=
NM_001025242.1:c.1540-43C=	NP_001020413.1:n.1540-43C=
NM_001025243.1:c.1350C=	NP_001020414.1:p.Pro450=
NM_001569.3:c.1587C=	NP_001560.2:p.Pro529=
XM_005274668.2:c.1618-43C=	XP_005274725.1:n.1618-43C=
XM_011531158.1:c.1303-43C=	XP_011529460.1:n.1303-43C=
XM_005274668.4:c.1618-43C=	XP_005274725.1:n.1618-43C=
NM_001569.4:c.1587C= MANE Select	NP_001560.2:p.Pro529=
NM_001025242.2:c.1540-43C=	NP_001020413.1:n.1540-43C=
NM_001025243.2:c.1350C=	NP_001020414.1:p.Pro450=