Canonical Allele Identifier: CA519268449

Gene: IRAK1

Linked Data

• gnomAD v4: X-154018749-G-A
• MyVariant Identifiers: chrX:g.153284200G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154018749G>A , CM000685.2:g.154018749G>A	GRCh38
NC_000023.10:g.153284200G>A , CM000685.1:g.153284200G>A	GRCh37
NC_000023.9:g.152937394G>A	NCBI36
NG_008387.1:g.6143C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000699980.1:n.123C>T
ENST00000369980.8:c.579C>T MANE Select	ENSP00000358997.3:p.Ala193=
ENST00000369973.7:c.657C>T	ENSP00000358990.3:p.Ala219=
ENST00000369974.6:c.579C>T	ENSP00000358991.2:p.Ala193=
ENST00000369980.7:c.579C>T	ENSP00000358997.3:p.Ala193=
ENST00000393687.6:c.579C>T	ENSP00000377291.2:p.Ala193=
ENST00000429936.6:c.657C>T	ENSP00000392662.2:p.Ala219=
ENST00000444230.5:c.528+226C>T	ENSP00000399974.1:n.528+226C>T
ENST00000463031.1:n.197C>T
NM_001025242.1:c.579C>T	NP_001020413.1:p.Ala193=
NM_001025243.1:c.579C>T	NP_001020414.1:p.Ala193=
NM_001569.3:c.579C>T	NP_001560.2:p.Ala193=
XM_005274668.2:c.657C>T	XP_005274725.1:p.Ala219=
XM_011531158.1:c.579C>T	XP_011529460.1:p.Ala193=
XM_005274668.4:c.657C>T	XP_005274725.1:p.Ala219=
NM_001569.4:c.579C>T MANE Select	NP_001560.2:p.Ala193=
NM_001025242.2:c.579C>T	NP_001020413.1:p.Ala193=
NM_001025243.2:c.579C>T	NP_001020414.1:p.Ala193=