Canonical Allele Identifier: CA519704003
Gene: IRAK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153278849C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154013398C>G , CM000685.2:g.154013398C>G GRCh38
NC_000023.10:g.153278849C>G , CM000685.1:g.153278849C>G GRCh37
NC_000023.9:g.152932043C>G NCBI36
NG_008387.1:g.11494G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000467236.2:n.355G>C
ENST00000699980.1:n.1119G>C
ENST00000369980.8:c.1575G>C MANE Select ENSP00000358997.3:p.Val525=
ENST00000369973.7:c.*518G>C ENSP00000358990.3:n.*518G>C
ENST00000369974.6:c.1338G>C ENSP00000358991.2:p.Val446=
ENST00000369980.7:c.1575G>C ENSP00000358997.3:p.Val525=
ENST00000393687.6:c.1540-55G>C ENSP00000377291.2:n.1540-55G>C
ENST00000429936.6:c.1618-55G>C ENSP00000392662.2:n.1618-55G>C
ENST00000437278.5:c.321-55G>C
ENST00000443220.1:c.820G>C
ENST00000444230.5:c.529-2282G>C ENSP00000399974.1:n.529-2282G>C
ENST00000444254.1:c.241G>C
ENST00000455690.5:c.279+644G>C ENSP00000411809.1:n.279+644G>C
ENST00000467236.1:n.372G>C
ENST00000477274.1:n.616-2587G>C
NM_001025242.1:c.1540-55G>C NP_001020413.1:n.1540-55G>C
NM_001025243.1:c.1338G>C NP_001020414.1:p.Val446=
NM_001569.3:c.1575G>C NP_001560.2:p.Val525=
XM_005274668.2:c.1618-55G>C XP_005274725.1:n.1618-55G>C
XM_011531158.1:c.1303-55G>C XP_011529460.1:n.1303-55G>C
XM_005274668.4:c.1618-55G>C XP_005274725.1:n.1618-55G>C
NM_001569.4:c.1575G>C MANE Select NP_001560.2:p.Val525=
NM_001025242.2:c.1540-55G>C NP_001020413.1:n.1540-55G>C
NM_001025243.2:c.1338G>C NP_001020414.1:p.Val446=