Canonical Allele Identifier: CA2466565208

Gene: IRAK1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154018642G= , CM000685.2:g.154018642G=	GRCh38
NC_000023.10:g.153284093G= , CM000685.1:g.153284093G=	GRCh37
NC_000023.9:g.152937287G=	NCBI36
NG_008387.1:g.6250C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699980.1:n.230C=
ENST00000369980.8:c.686C= MANE Select	ENSP00000358997.3:p.Ala229=
ENST00000369973.7:c.764C=	ENSP00000358990.3:p.Ala255=
ENST00000369974.6:c.686C=	ENSP00000358991.2:p.Ala229=
ENST00000369980.7:c.686C=	ENSP00000358997.3:p.Ala229=
ENST00000393687.6:c.686C=	ENSP00000377291.2:p.Ala229=
ENST00000429936.6:c.764C=	ENSP00000392662.2:p.Ala255=
ENST00000444230.5:c.528+333C=	ENSP00000399974.1:n.528+333C=
ENST00000463031.1:n.304C=
ENST00000477274.1:n.6C=
NM_001025242.1:c.686C=	NP_001020413.1:p.Ala229=
NM_001025243.1:c.686C=	NP_001020414.1:p.Ala229=
NM_001569.3:c.686C=	NP_001560.2:p.Ala229=
XM_005274668.2:c.764C=	XP_005274725.1:p.Ala255=
XM_011531158.1:c.686C=	XP_011529460.1:p.Ala229=
XM_005274668.4:c.764C=	XP_005274725.1:p.Ala255=
NM_001569.4:c.686C= MANE Select	NP_001560.2:p.Ala229=
NM_001025242.2:c.686C=	NP_001020413.1:p.Ala229=
NM_001025243.2:c.686C=	NP_001020414.1:p.Ala229=