Canonical Allele Identifier: CA519704377

Gene: IRAK1

Linked Data

• MyVariant Identifiers: chrX:g.153278831A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154013380A>G , CM000685.2:g.154013380A>G	GRCh38
NC_000023.10:g.153278831A>G , CM000685.1:g.153278831A>G	GRCh37
NC_000023.9:g.152932025A>G	NCBI36
NG_008387.1:g.11512T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467236.2:n.373T>C
ENST00000699980.1:n.1137T>C
ENST00000369980.8:c.1593T>C MANE Select	ENSP00000358997.3:p.His531=
ENST00000369973.7:c.*536T>C	ENSP00000358990.3:n.*536T>C
ENST00000369974.6:c.1356T>C	ENSP00000358991.2:p.His452=
ENST00000369980.7:c.1593T>C	ENSP00000358997.3:p.His531=
ENST00000393687.6:c.1540-37T>C	ENSP00000377291.2:n.1540-37T>C
ENST00000429936.6:c.1618-37T>C	ENSP00000392662.2:n.1618-37T>C
ENST00000437278.5:c.321-37T>C
ENST00000443220.1:c.838T>C
ENST00000444230.5:c.529-2264T>C	ENSP00000399974.1:n.529-2264T>C
ENST00000444254.1:c.259T>C
ENST00000455690.5:c.279+662T>C	ENSP00000411809.1:n.279+662T>C
ENST00000467236.1:n.390T>C
ENST00000477274.1:n.616-2569T>C
NM_001025242.1:c.1540-37T>C	NP_001020413.1:n.1540-37T>C
NM_001025243.1:c.1356T>C	NP_001020414.1:p.His452=
NM_001569.3:c.1593T>C	NP_001560.2:p.His531=
XM_005274668.2:c.1618-37T>C	XP_005274725.1:n.1618-37T>C
XM_011531158.1:c.1303-37T>C	XP_011529460.1:n.1303-37T>C
XM_005274668.4:c.1618-37T>C	XP_005274725.1:n.1618-37T>C
NM_001569.4:c.1593T>C MANE Select	NP_001560.2:p.His531=
NM_001025242.2:c.1540-37T>C	NP_001020413.1:n.1540-37T>C
NM_001025243.2:c.1356T>C	NP_001020414.1:p.His452=