Canonical Allele Identifier: CA415139708
Gene: IRAK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154013291C>A , CM000685.2:g.154013291C>A GRCh38
NC_000023.10:g.153278742C>A , CM000685.1:g.153278742C>A GRCh37
NC_000023.9:g.152931936C>A NCBI36
NG_008387.1:g.11601G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000467236.2:n.462G>T
ENST00000699980.1:n.1226G>T
ENST00000369980.8:c.1682G>T MANE Select ENSP00000358997.3:p.Trp561Leu
ENST00000369973.7:c.*625G>T ENSP00000358990.3:n.*625G>T
ENST00000369974.6:c.1445G>T ENSP00000358991.2:p.Trp482Leu
ENST00000369980.7:c.1682G>T ENSP00000358997.3:p.Trp561Leu
ENST00000393687.6:c.1592G>T ENSP00000377291.2:p.Trp531Leu
ENST00000429936.6:c.1670G>T ENSP00000392662.2:p.Trp557Leu
ENST00000437278.5:c.373G>T
ENST00000443220.1:c.927G>T
ENST00000444230.5:c.529-2175G>T ENSP00000399974.1:n.529-2175G>T
ENST00000444254.1:c.348G>T
ENST00000455690.5:c.280-613G>T ENSP00000411809.1:n.280-613G>T
ENST00000477274.1:n.616-2480G>T
NM_001025242.1:c.1592G>T NP_001020413.1:p.Trp531Leu
NM_001025243.1:c.1445G>T NP_001020414.1:p.Trp482Leu
NM_001569.3:c.1682G>T NP_001560.2:p.Trp561Leu
XM_005274668.2:c.1670G>T XP_005274725.1:p.Trp557Leu
XM_011531158.1:c.1355G>T XP_011529460.1:p.Trp452Leu
XM_005274668.4:c.1670G>T XP_005274725.1:p.Trp557Leu
NM_001569.4:c.1682G>T MANE Select NP_001560.2:p.Trp561Leu
NM_001025242.2:c.1592G>T NP_001020413.1:p.Trp531Leu
NM_001025243.2:c.1445G>T NP_001020414.1:p.Trp482Leu