Canonical Allele Identifier: CA2239533964
Community Standard Title: NM_002163.4(IRF8):c.238A= (p.Thr80=)
Gene: IRF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.85909053A= , CM000678.2:g.85909053A= GRCh38
NC_000016.9:g.85942659A= , CM000678.1:g.85942659A= GRCh37
NC_000016.8:g.84500160A= NCBI36
NG_029333.1:g.14886A= , LRG_294:g.14886A=

Transcript Alleles

HGVS Amino-acid Change
NM_002163.4:c.238A= MANE Select NP_002154.1:p.Thr80=
ENST00000268638.10:c.238A= MANE Select ENSP00000268638.4:p.Thr80=
NM_001363907.1:c.268A= NP_001350836.1:p.Thr90=
NM_001363908.1:c.-269A= NP_001350837.1:n.-269A=
NM_002163.2:c.238A= , LRG_294t1:c.238A= NP_002154.1:p.Thr80=
NM_002163.3:c.238A= NP_002154.1:p.Thr80=
ENST00000268638.9:c.238A= ENSP00000268638.4:p.Thr80=
ENST00000563180.1:c.238A= ENSP00000458047.1:p.Thr80=
ENST00000564056.1:n.123A=
ENST00000564617.5:c.238A= ENSP00000455784.1:p.Thr80=
ENST00000564803.5:c.238A= ENSP00000456992.1:p.Thr80=
ENST00000564803.6:c.238A= ENSP00000456992.2:p.Thr80=
ENST00000566369.1:c.66A=
ENST00000566369.2:c.238A= ENSP00000455048.2:p.Thr80=
ENST00000696884.1:c.238A= ENSP00000512951.1:p.Thr80=
ENST00000696885.1:c.238A= ENSP00000512952.1:p.Thr80=
ENST00000696886.1:n.288A=
ENST00000696887.1:c.238A= ENSP00000512953.1:p.Thr80=
ENST00000696888.1:n.287A=
ENST00000696889.1:n.231A=
ENST00000696890.1:n.185A=