Canonical Allele Identifier: CA519268277

Gene: IRAK1

Linked Data

• MyVariant Identifiers: chrX:g.153284101C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154018650C>T , CM000685.2:g.154018650C>T	GRCh38
NC_000023.10:g.153284101C>T , CM000685.1:g.153284101C>T	GRCh37
NC_000023.9:g.152937295C>T	NCBI36
NG_008387.1:g.6242G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000699980.1:n.222G>A
ENST00000369980.8:c.678G>A MANE Select	ENSP00000358997.3:p.Val226=
ENST00000369973.7:c.756G>A	ENSP00000358990.3:p.Val252=
ENST00000369974.6:c.678G>A	ENSP00000358991.2:p.Val226=
ENST00000369980.7:c.678G>A	ENSP00000358997.3:p.Val226=
ENST00000393687.6:c.678G>A	ENSP00000377291.2:p.Val226=
ENST00000429936.6:c.756G>A	ENSP00000392662.2:p.Val252=
ENST00000444230.5:c.528+325G>A	ENSP00000399974.1:n.528+325G>A
ENST00000463031.1:n.296G>A
NM_001025242.1:c.678G>A	NP_001020413.1:p.Val226=
NM_001025243.1:c.678G>A	NP_001020414.1:p.Val226=
NM_001569.3:c.678G>A	NP_001560.2:p.Val226=
XM_005274668.2:c.756G>A	XP_005274725.1:p.Val252=
XM_011531158.1:c.678G>A	XP_011529460.1:p.Val226=
XM_005274668.4:c.756G>A	XP_005274725.1:p.Val252=
NM_001569.4:c.678G>A MANE Select	NP_001560.2:p.Val226=
NM_001025242.2:c.678G>A	NP_001020413.1:p.Val226=
NM_001025243.2:c.678G>A	NP_001020414.1:p.Val226=