Canonical Allele Identifier: CA415139662

Gene: IRAK1

Linked Data

• MyVariant Identifiers: chrX:g.153278737G>T (hg19) ; chrX:g.154013286G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154013286G>T , CM000685.2:g.154013286G>T	GRCh38
NC_000023.10:g.153278737G>T , CM000685.1:g.153278737G>T	GRCh37
NC_000023.9:g.152931931G>T	NCBI36
NG_008387.1:g.11606C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467236.2:n.467C>A
ENST00000699980.1:n.1231C>A
ENST00000369980.8:c.1687C>A MANE Select	ENSP00000358997.3:p.Pro563Thr
ENST00000369973.7:c.*630C>A	ENSP00000358990.3:n.*630C>A
ENST00000369974.6:c.1450C>A	ENSP00000358991.2:p.Pro484Thr
ENST00000369980.7:c.1687C>A	ENSP00000358997.3:p.Pro563Thr
ENST00000393687.6:c.1597C>A	ENSP00000377291.2:p.Pro533Thr
ENST00000429936.6:c.1675C>A	ENSP00000392662.2:p.Pro559Thr
ENST00000437278.5:c.378C>A
ENST00000443220.1:c.932C>A
ENST00000444230.5:c.529-2170C>A	ENSP00000399974.1:n.529-2170C>A
ENST00000444254.1:c.353C>A
ENST00000455690.5:c.280-608C>A	ENSP00000411809.1:n.280-608C>A
ENST00000477274.1:n.616-2475C>A
NM_001025242.1:c.1597C>A	NP_001020413.1:p.Pro533Thr
NM_001025243.1:c.1450C>A	NP_001020414.1:p.Pro484Thr
NM_001569.3:c.1687C>A	NP_001560.2:p.Pro563Thr
XM_005274668.2:c.1675C>A	XP_005274725.1:p.Pro559Thr
XM_011531158.1:c.1360C>A	XP_011529460.1:p.Pro454Thr
XM_005274668.4:c.1675C>A	XP_005274725.1:p.Pro559Thr
NM_001569.4:c.1687C>A MANE Select	NP_001560.2:p.Pro563Thr
NM_001025242.2:c.1597C>A	NP_001020413.1:p.Pro533Thr
NM_001025243.2:c.1450C>A	NP_001020414.1:p.Pro484Thr