Canonical Allele Identifier: CA2332659527
Gene: CEBPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33300449_33300451delinsGGA , CM000681.2:g.33300449_33300451delinsGGA GRCh38
NC_000019.9:g.33791355_33791357delinsGGA , CM000681.1:g.33791355_33791357delinsGGA GRCh37
NC_000019.8:g.38483195_38483197delinsGGA NCBI36
NG_012022.1:g.7074_7076delinsTCC , LRG_456:g.7074_7076delinsTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.*887_*889delinsTCC MANE Select ENSP00000427514.1:n.*887_*889delinsTCC
ENST00000498907.2:c.*887_*889delinsTCC ENSP00000427514.1:n.*887_*889delinsTCC
NM_001285829.1:c.*887_*889delinsTCC NP_001272758.1:n.*887_*889delinsTCC
NM_001287424.1:c.*887_*889delinsTCC NP_001274353.1:n.*887_*889delinsTCC
NM_001287435.1:c.*887_*889delinsTCC NP_001274364.1:n.*887_*889delinsTCC
NM_004364.4:c.*887_*889delinsTCC NP_004355.2:n.*887_*889delinsTCC
NM_001287424.2:c.*887_*889delinsTCC NP_001274353.1:n.*887_*889delinsTCC
NM_004364.5:c.*887_*889delinsTCC MANE Select NP_004355.2:n.*887_*889delinsTCC
NM_001285829.2:c.*887_*889delinsTCC NP_001272758.1:n.*887_*889delinsTCC
NM_001287435.2:c.*887_*889delinsTCC NP_001274364.1:n.*887_*889delinsTCC