Canonical Allele Identifier: CA2332659472
Gene: CEBPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33300293_33300297delinsAAAAC , CM000681.2:g.33300293_33300297delinsAAAAC GRCh38
NC_000019.9:g.33791199_33791203delinsAAAAC , CM000681.1:g.33791199_33791203delinsAAAAC GRCh37
NC_000019.8:g.38483039_38483043delinsAAAAC NCBI36
NG_012022.1:g.7228_7232delinsGTTTT , LRG_456:g.7228_7232delinsGTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.*1041_*1045delinsGTTTT MANE Select ENSP00000427514.1:n.*1041_*1045delinsGTTTT
ENST00000498907.2:c.*1041_*1045delinsGTTTT ENSP00000427514.1:n.*1041_*1045delinsGTTTT
NM_001285829.1:c.*1041_*1045delinsGTTTT NP_001272758.1:n.*1041_*1045delinsGTTTT
NM_001287424.1:c.*1041_*1045delinsGTTTT NP_001274353.1:n.*1041_*1045delinsGTTTT
NM_001287435.1:c.*1041_*1045delinsGTTTT NP_001274364.1:n.*1041_*1045delinsGTTTT
NM_004364.4:c.*1041_*1045delinsGTTTT NP_004355.2:n.*1041_*1045delinsGTTTT
NM_001287424.2:c.*1041_*1045delinsGTTTT NP_001274353.1:n.*1041_*1045delinsGTTTT
NM_004364.5:c.*1041_*1045delinsGTTTT MANE Select NP_004355.2:n.*1041_*1045delinsGTTTT
NM_001285829.2:c.*1041_*1045delinsGTTTT NP_001272758.1:n.*1041_*1045delinsGTTTT
NM_001287435.2:c.*1041_*1045delinsGTTTT NP_001274364.1:n.*1041_*1045delinsGTTTT