Canonical Allele Identifier: CA2584317315

Gene: CEBPA

Linked Data

• gnomAD v4: 19-33300276-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33300276_33300277insT , CM000681.2:g.33300276_33300277insT	GRCh38
NC_000019.9:g.33791182_33791183insT , CM000681.1:g.33791182_33791183insT	GRCh37
NC_000019.8:g.38483022_38483023insT	NCBI36
NG_012022.1:g.7248_7249insA , LRG_456:g.7248_7249insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.*1061_*1062insA MANE Select	ENSP00000427514.1:n.*1061_*1062insA
ENST00000498907.2:c.*1061_*1062insA	ENSP00000427514.1:n.*1061_*1062insA
NM_001285829.1:c.*1061_*1062insA	NP_001272758.1:n.*1061_*1062insA
NM_001287424.1:c.*1061_*1062insA	NP_001274353.1:n.*1061_*1062insA
NM_001287435.1:c.*1061_*1062insA	NP_001274364.1:n.*1061_*1062insA
NM_004364.4:c.*1061_*1062insA	NP_004355.2:n.*1061_*1062insA
NM_001287424.2:c.*1061_*1062insA	NP_001274353.1:n.*1061_*1062insA
NM_004364.5:c.*1061_*1062insA MANE Select	NP_004355.2:n.*1061_*1062insA
NM_001285829.2:c.*1061_*1062insA	NP_001272758.1:n.*1061_*1062insA
NM_001287435.2:c.*1061_*1062insA	NP_001274364.1:n.*1061_*1062insA