Canonical Allele Identifier: CA2695198167

Gene: CEBPA

Linked Data

• ClinVar Variation Id: 2680565
• ClinVar RCV Id: RCV003460388

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33301897_33301962del , CM000681.2:g.33301897_33301962del	GRCh38
NC_000019.9:g.33792803_33792868del , CM000681.1:g.33792803_33792868del	GRCh37
NC_000019.8:g.38484643_38484708del	NCBI36
NG_012022.1:g.5568_5633del , LRG_456:g.5568_5633del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.458_523del MANE Select	ENSP00000427514.1:p.Pro153_Ala174del
ENST00000498907.2:c.458_523del	ENSP00000427514.1:p.Pro153_Ala174del
NM_001285829.1:c.101_166del	NP_001272758.1:p.Pro34_Ala55del
NM_001287424.1:c.563_628del	NP_001274353.1:p.Pro188_Ala209del
NM_001287435.1:c.416_481del	NP_001274364.1:p.Pro139_Ala160del
NM_004364.4:c.458_523del	NP_004355.2:p.Pro153_Ala174del
NM_001287424.2:c.563_628del	NP_001274353.1:p.Pro188_Ala209del
NM_004364.5:c.458_523del MANE Select	NP_004355.2:p.Pro153_Ala174del
NM_001285829.2:c.101_166del	NP_001272758.1:p.Pro34_Ala55del
NM_001287435.2:c.416_481del	NP_001274364.1:p.Pro139_Ala160del