Canonical Allele Identifier: CA415151444

Gene: IRAK1

Linked Data

• MyVariant Identifiers: chrX:g.153284199G>C (hg19) ; chrX:g.154018748G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154018748G>C , CM000685.2:g.154018748G>C	GRCh38
NC_000023.10:g.153284199G>C , CM000685.1:g.153284199G>C	GRCh37
NC_000023.9:g.152937393G>C	NCBI36
NG_008387.1:g.6144C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000699980.1:n.124C>G
ENST00000369980.8:c.580C>G MANE Select	ENSP00000358997.3:p.Arg194Gly
ENST00000369973.7:c.658C>G	ENSP00000358990.3:p.Arg220Gly
ENST00000369974.6:c.580C>G	ENSP00000358991.2:p.Arg194Gly
ENST00000369980.7:c.580C>G	ENSP00000358997.3:p.Arg194Gly
ENST00000393687.6:c.580C>G	ENSP00000377291.2:p.Arg194Gly
ENST00000429936.6:c.658C>G	ENSP00000392662.2:p.Arg220Gly
ENST00000444230.5:c.528+227C>G	ENSP00000399974.1:n.528+227C>G
ENST00000463031.1:n.198C>G
NM_001025242.1:c.580C>G	NP_001020413.1:p.Arg194Gly
NM_001025243.1:c.580C>G	NP_001020414.1:p.Arg194Gly
NM_001569.3:c.580C>G	NP_001560.2:p.Arg194Gly
XM_005274668.2:c.658C>G	XP_005274725.1:p.Arg220Gly
XM_011531158.1:c.580C>G	XP_011529460.1:p.Arg194Gly
XM_005274668.4:c.658C>G	XP_005274725.1:p.Arg220Gly
NM_001569.4:c.580C>G MANE Select	NP_001560.2:p.Arg194Gly
NM_001025242.2:c.580C>G	NP_001020413.1:p.Arg194Gly
NM_001025243.2:c.580C>G	NP_001020414.1:p.Arg194Gly