Canonical Allele Identifier: CA415139568

Gene: IRAK1

Linked Data

• MyVariant Identifiers: chrX:g.153278734G>T (hg19) ; chrX:g.154013283G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154013283G>T , CM000685.2:g.154013283G>T	GRCh38
NC_000023.10:g.153278734G>T , CM000685.1:g.153278734G>T	GRCh37
NC_000023.9:g.152931928G>T	NCBI36
NG_008387.1:g.11609C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467236.2:n.470C>A
ENST00000699980.1:n.1234C>A
ENST00000369980.8:c.1690C>A MANE Select	ENSP00000358997.3:p.Leu564Met
ENST00000369973.7:c.*633C>A	ENSP00000358990.3:n.*633C>A
ENST00000369974.6:c.1453C>A	ENSP00000358991.2:p.Leu485Met
ENST00000369980.7:c.1690C>A	ENSP00000358997.3:p.Leu564Met
ENST00000393687.6:c.1600C>A	ENSP00000377291.2:p.Leu534Met
ENST00000429936.6:c.1678C>A	ENSP00000392662.2:p.Leu560Met
ENST00000437278.5:c.381C>A
ENST00000443220.1:c.935C>A
ENST00000444230.5:c.529-2167C>A	ENSP00000399974.1:n.529-2167C>A
ENST00000444254.1:c.356C>A
ENST00000455690.5:c.280-605C>A	ENSP00000411809.1:n.280-605C>A
ENST00000477274.1:n.616-2472C>A
NM_001025242.1:c.1600C>A	NP_001020413.1:p.Leu534Met
NM_001025243.1:c.1453C>A	NP_001020414.1:p.Leu485Met
NM_001569.3:c.1690C>A	NP_001560.2:p.Leu564Met
XM_005274668.2:c.1678C>A	XP_005274725.1:p.Leu560Met
XM_011531158.1:c.1363C>A	XP_011529460.1:p.Leu455Met
XM_005274668.4:c.1678C>A	XP_005274725.1:p.Leu560Met
NM_001569.4:c.1690C>A MANE Select	NP_001560.2:p.Leu564Met
NM_001025242.2:c.1600C>A	NP_001020413.1:p.Leu534Met
NM_001025243.2:c.1453C>A	NP_001020414.1:p.Leu485Met