Canonical Allele Identifier: CA415140893

Gene: IRAK1

Linked Data

• MyVariant Identifiers: chrX:g.153278838G>A (hg19) ; chrX:g.154013387G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154013387G>A , CM000685.2:g.154013387G>A	GRCh38
NC_000023.10:g.153278838G>A , CM000685.1:g.153278838G>A	GRCh37
NC_000023.9:g.152932032G>A	NCBI36
NG_008387.1:g.11505C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467236.2:n.366C>T
ENST00000699980.1:n.1130C>T
ENST00000369980.8:c.1586C>T MANE Select	ENSP00000358997.3:p.Pro529Leu
ENST00000369973.7:c.*529C>T	ENSP00000358990.3:n.*529C>T
ENST00000369974.6:c.1349C>T	ENSP00000358991.2:p.Pro450Leu
ENST00000369980.7:c.1586C>T	ENSP00000358997.3:p.Pro529Leu
ENST00000393687.6:c.1540-44C>T	ENSP00000377291.2:n.1540-44C>T
ENST00000429936.6:c.1618-44C>T	ENSP00000392662.2:n.1618-44C>T
ENST00000437278.5:c.321-44C>T
ENST00000443220.1:c.831C>T
ENST00000444230.5:c.529-2271C>T	ENSP00000399974.1:n.529-2271C>T
ENST00000444254.1:c.252C>T
ENST00000455690.5:c.279+655C>T	ENSP00000411809.1:n.279+655C>T
ENST00000467236.1:n.383C>T
ENST00000477274.1:n.616-2576C>T
NM_001025242.1:c.1540-44C>T	NP_001020413.1:n.1540-44C>T
NM_001025243.1:c.1349C>T	NP_001020414.1:p.Pro450Leu
NM_001569.3:c.1586C>T	NP_001560.2:p.Pro529Leu
XM_005274668.2:c.1618-44C>T	XP_005274725.1:n.1618-44C>T
XM_011531158.1:c.1303-44C>T	XP_011529460.1:n.1303-44C>T
XM_005274668.4:c.1618-44C>T	XP_005274725.1:n.1618-44C>T
NM_001569.4:c.1586C>T MANE Select	NP_001560.2:p.Pro529Leu
NM_001025242.2:c.1540-44C>T	NP_001020413.1:n.1540-44C>T
NM_001025243.2:c.1349C>T	NP_001020414.1:p.Pro450Leu