Canonical Allele Identifier: CA2332659497
Gene: CEBPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33300359C= , CM000681.2:g.33300359C= GRCh38
NC_000019.9:g.33791265C= , CM000681.1:g.33791265C= GRCh37
NC_000019.8:g.38483105C= NCBI36
NG_012022.1:g.7166G= , LRG_456:g.7166G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.*979G= MANE Select ENSP00000427514.1:n.*979G=
ENST00000498907.2:c.*979G= ENSP00000427514.1:n.*979G=
NM_001285829.1:c.*979G= NP_001272758.1:n.*979G=
NM_001287424.1:c.*979G= NP_001274353.1:n.*979G=
NM_001287435.1:c.*979G= NP_001274364.1:n.*979G=
NM_004364.4:c.*979G= NP_004355.2:n.*979G=
NM_001287424.2:c.*979G= NP_001274353.1:n.*979G=
NM_004364.5:c.*979G= MANE Select NP_004355.2:n.*979G=
NM_001285829.2:c.*979G= NP_001272758.1:n.*979G=
NM_001287435.2:c.*979G= NP_001274364.1:n.*979G=