Canonical Allele Identifier: CA2697556437

Gene: CEBPA

Linked Data

• ClinVar Variation Id: 2767496
• ClinVar RCV Id: RCV003517742

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33302367_33302369del , CM000681.2:g.33302367_33302369del	GRCh38
NC_000019.9:g.33793273_33793275del , CM000681.1:g.33793273_33793275del	GRCh37
NC_000019.8:g.38485113_38485115del	NCBI36
NG_012022.1:g.5159_5161del , LRG_456:g.5159_5161del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.49_51del MANE Select	ENSP00000427514.1:p.Ser17del
ENST00000498907.2:c.49_51del	ENSP00000427514.1:p.Ser17del
NM_001285829.1:c.-309_-307del	NP_001272758.1:n.-309_-307del
NM_001287424.1:c.154_156del	NP_001274353.1:p.Ser52del
NM_001287435.1:c.7_9del	NP_001274364.1:p.Ser3del
NM_004364.4:c.49_51del	NP_004355.2:p.Ser17del
NM_001287424.2:c.154_156del	NP_001274353.1:p.Ser52del
NM_004364.5:c.49_51del MANE Select	NP_004355.2:p.Ser17del
NM_001285829.2:c.-309_-307del	NP_001272758.1:n.-309_-307del
NM_001287435.2:c.7_9del	NP_001274364.1:p.Ser3del