Canonical Allele Identifier: CA519704265

Gene: IRAK1

Linked Data

• MyVariant Identifiers: chrX:g.153278735G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154013284G>A , CM000685.2:g.154013284G>A	GRCh38
NC_000023.10:g.153278735G>A , CM000685.1:g.153278735G>A	GRCh37
NC_000023.9:g.152931929G>A	NCBI36
NG_008387.1:g.11608C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467236.2:n.469C>T
ENST00000699980.1:n.1233C>T
ENST00000369980.8:c.1689C>T MANE Select	ENSP00000358997.3:p.Pro563=
ENST00000369973.7:c.*632C>T	ENSP00000358990.3:n.*632C>T
ENST00000369974.6:c.1452C>T	ENSP00000358991.2:p.Pro484=
ENST00000369980.7:c.1689C>T	ENSP00000358997.3:p.Pro563=
ENST00000393687.6:c.1599C>T	ENSP00000377291.2:p.Pro533=
ENST00000429936.6:c.1677C>T	ENSP00000392662.2:p.Pro559=
ENST00000437278.5:c.380C>T
ENST00000443220.1:c.934C>T
ENST00000444230.5:c.529-2168C>T	ENSP00000399974.1:n.529-2168C>T
ENST00000444254.1:c.355C>T
ENST00000455690.5:c.280-606C>T	ENSP00000411809.1:n.280-606C>T
ENST00000477274.1:n.616-2473C>T
NM_001025242.1:c.1599C>T	NP_001020413.1:p.Pro533=
NM_001025243.1:c.1452C>T	NP_001020414.1:p.Pro484=
NM_001569.3:c.1689C>T	NP_001560.2:p.Pro563=
XM_005274668.2:c.1677C>T	XP_005274725.1:p.Pro559=
XM_011531158.1:c.1362C>T	XP_011529460.1:p.Pro454=
XM_005274668.4:c.1677C>T	XP_005274725.1:p.Pro559=
NM_001569.4:c.1689C>T MANE Select	NP_001560.2:p.Pro563=
NM_001025242.2:c.1599C>T	NP_001020413.1:p.Pro533=
NM_001025243.2:c.1452C>T	NP_001020414.1:p.Pro484=