Canonical Allele Identifier: CA415141332

Gene: IRAK1

Linked Data

• COSMIC: COSM1644683 ; COSM1644684
• MyVariant Identifiers: chrX:g.153278880T>C (hg19) ; chrX:g.154013429T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154013429T>C , CM000685.2:g.154013429T>C	GRCh38
NC_000023.10:g.153278880T>C , CM000685.1:g.153278880T>C	GRCh37
NC_000023.9:g.152932074T>C	NCBI36
NG_008387.1:g.11463A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467236.2:n.324A>G
ENST00000699980.1:n.1088A>G
ENST00000369980.8:c.1544A>G MANE Select	ENSP00000358997.3:p.Tyr515Cys
ENST00000369973.7:c.*487A>G	ENSP00000358990.3:n.*487A>G
ENST00000369974.6:c.1307A>G	ENSP00000358991.2:p.Tyr436Cys
ENST00000369980.7:c.1544A>G	ENSP00000358997.3:p.Tyr515Cys
ENST00000393687.6:c.1540-86A>G	ENSP00000377291.2:n.1540-86A>G
ENST00000429936.6:c.1618-86A>G	ENSP00000392662.2:n.1618-86A>G
ENST00000437278.5:c.321-86A>G
ENST00000443220.1:c.789A>G
ENST00000444230.5:c.529-2313A>G	ENSP00000399974.1:n.529-2313A>G
ENST00000444254.1:c.210A>G
ENST00000455690.5:c.279+613A>G	ENSP00000411809.1:n.279+613A>G
ENST00000467236.1:n.341A>G
ENST00000477274.1:n.615+2610A>G
NM_001025242.1:c.1540-86A>G	NP_001020413.1:n.1540-86A>G
NM_001025243.1:c.1307A>G	NP_001020414.1:p.Tyr436Cys
NM_001569.3:c.1544A>G	NP_001560.2:p.Tyr515Cys
XM_005274668.2:c.1618-86A>G	XP_005274725.1:n.1618-86A>G
XM_011531158.1:c.1303-86A>G	XP_011529460.1:n.1303-86A>G
XM_005274668.4:c.1618-86A>G	XP_005274725.1:n.1618-86A>G
NM_001569.4:c.1544A>G MANE Select	NP_001560.2:p.Tyr515Cys
NM_001025242.2:c.1540-86A>G	NP_001020413.1:n.1540-86A>G
NM_001025243.2:c.1307A>G	NP_001020414.1:p.Tyr436Cys