Canonical Allele Identifier: CA2332659468
Gene: CEBPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33300288A= , CM000681.2:g.33300288A= GRCh38
NC_000019.9:g.33791194A= , CM000681.1:g.33791194A= GRCh37
NC_000019.8:g.38483034A= NCBI36
NG_012022.1:g.7237T= , LRG_456:g.7237T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.*1050T= MANE Select ENSP00000427514.1:n.*1050T=
ENST00000498907.2:c.*1050T= ENSP00000427514.1:n.*1050T=
NM_001285829.1:c.*1050T= NP_001272758.1:n.*1050T=
NM_001287424.1:c.*1050T= NP_001274353.1:n.*1050T=
NM_001287435.1:c.*1050T= NP_001274364.1:n.*1050T=
NM_004364.4:c.*1050T= NP_004355.2:n.*1050T=
NM_001287424.2:c.*1050T= NP_001274353.1:n.*1050T=
NM_004364.5:c.*1050T= MANE Select NP_004355.2:n.*1050T=
NM_001285829.2:c.*1050T= NP_001272758.1:n.*1050T=
NM_001287435.2:c.*1050T= NP_001274364.1:n.*1050T=