Canonical Allele Identifier: CA519704263

Gene: IRAK1

Linked Data

• MyVariant Identifiers: chrX:g.153278732C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154013281C>G , CM000685.2:g.154013281C>G	GRCh38
NC_000023.10:g.153278732C>G , CM000685.1:g.153278732C>G	GRCh37
NC_000023.9:g.152931926C>G	NCBI36
NG_008387.1:g.11611G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467236.2:n.472G>C
ENST00000699980.1:n.1236G>C
ENST00000369980.8:c.1692G>C MANE Select	ENSP00000358997.3:p.Leu564=
ENST00000369973.7:c.*635G>C	ENSP00000358990.3:n.*635G>C
ENST00000369974.6:c.1455G>C	ENSP00000358991.2:p.Leu485=
ENST00000369980.7:c.1692G>C	ENSP00000358997.3:p.Leu564=
ENST00000393687.6:c.1602G>C	ENSP00000377291.2:p.Leu534=
ENST00000429936.6:c.1680G>C	ENSP00000392662.2:p.Leu560=
ENST00000437278.5:c.383G>C
ENST00000443220.1:c.937G>C
ENST00000444230.5:c.529-2165G>C	ENSP00000399974.1:n.529-2165G>C
ENST00000444254.1:c.358G>C
ENST00000455690.5:c.280-603G>C	ENSP00000411809.1:n.280-603G>C
ENST00000477274.1:n.616-2470G>C
NM_001025242.1:c.1602G>C	NP_001020413.1:p.Leu534=
NM_001025243.1:c.1455G>C	NP_001020414.1:p.Leu485=
NM_001569.3:c.1692G>C	NP_001560.2:p.Leu564=
XM_005274668.2:c.1680G>C	XP_005274725.1:p.Leu560=
XM_011531158.1:c.1365G>C	XP_011529460.1:p.Leu455=
XM_005274668.4:c.1680G>C	XP_005274725.1:p.Leu560=
NM_001569.4:c.1692G>C MANE Select	NP_001560.2:p.Leu564=
NM_001025242.2:c.1602G>C	NP_001020413.1:p.Leu534=
NM_001025243.2:c.1455G>C	NP_001020414.1:p.Leu485=