Canonical Allele Identifier: CA415150375

Gene: IRAK1

Linked Data

• MyVariant Identifiers: chrX:g.153284094C>G (hg19) ; chrX:g.154018643C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154018643C>G , CM000685.2:g.154018643C>G	GRCh38
NC_000023.10:g.153284094C>G , CM000685.1:g.153284094C>G	GRCh37
NC_000023.9:g.152937288C>G	NCBI36
NG_008387.1:g.6249G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000699980.1:n.229G>C
ENST00000369980.8:c.685G>C MANE Select	ENSP00000358997.3:p.Ala229Pro
ENST00000369973.7:c.763G>C	ENSP00000358990.3:p.Ala255Pro
ENST00000369974.6:c.685G>C	ENSP00000358991.2:p.Ala229Pro
ENST00000369980.7:c.685G>C	ENSP00000358997.3:p.Ala229Pro
ENST00000393687.6:c.685G>C	ENSP00000377291.2:p.Ala229Pro
ENST00000429936.6:c.763G>C	ENSP00000392662.2:p.Ala255Pro
ENST00000444230.5:c.528+332G>C	ENSP00000399974.1:n.528+332G>C
ENST00000463031.1:n.303G>C
ENST00000477274.1:n.5G>C
NM_001025242.1:c.685G>C	NP_001020413.1:p.Ala229Pro
NM_001025243.1:c.685G>C	NP_001020414.1:p.Ala229Pro
NM_001569.3:c.685G>C	NP_001560.2:p.Ala229Pro
XM_005274668.2:c.763G>C	XP_005274725.1:p.Ala255Pro
XM_011531158.1:c.685G>C	XP_011529460.1:p.Ala229Pro
XM_005274668.4:c.763G>C	XP_005274725.1:p.Ala255Pro
NM_001569.4:c.685G>C MANE Select	NP_001560.2:p.Ala229Pro
NM_001025242.2:c.685G>C	NP_001020413.1:p.Ala229Pro
NM_001025243.2:c.685G>C	NP_001020414.1:p.Ala229Pro