Canonical Allele Identifier: CA2332659491
Gene: CEBPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33300335A= , CM000681.2:g.33300335A= GRCh38
NC_000019.9:g.33791241A= , CM000681.1:g.33791241A= GRCh37
NC_000019.8:g.38483081A= NCBI36
NG_012022.1:g.7190T= , LRG_456:g.7190T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.*1003T= MANE Select ENSP00000427514.1:n.*1003T=
ENST00000498907.2:c.*1003T= ENSP00000427514.1:n.*1003T=
NM_001285829.1:c.*1003T= NP_001272758.1:n.*1003T=
NM_001287424.1:c.*1003T= NP_001274353.1:n.*1003T=
NM_001287435.1:c.*1003T= NP_001274364.1:n.*1003T=
NM_004364.4:c.*1003T= NP_004355.2:n.*1003T=
NM_001287424.2:c.*1003T= NP_001274353.1:n.*1003T=
NM_004364.5:c.*1003T= MANE Select NP_004355.2:n.*1003T=
NM_001285829.2:c.*1003T= NP_001272758.1:n.*1003T=
NM_001287435.2:c.*1003T= NP_001274364.1:n.*1003T=