Canonical Allele Identifier: CA507007617
Gene: CEBPA HGNC NCBI

Linked Data

COSMIC: COSM29488
MyVariant Identifiers: chr19:g.33793160del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33302255del , CM000681.2:g.33302255del GRCh38
NC_000019.9:g.33793161del , CM000681.1:g.33793161del GRCh37
NC_000019.8:g.38485001del NCBI36
NG_012022.1:g.5271del , LRG_456:g.5271del

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.161del MANE Select ENSP00000427514.1:p.Gly54AlafsTer?
ENST00000498907.2:c.161del ENSP00000427514.1:p.Gly54AlafsTer?
NM_001285829.1:c.-197del NP_001272758.1:n.-197del
NM_001287424.1:c.266del NP_001274353.1:p.Gly89AlafsTer?
NM_001287435.1:c.119del NP_001274364.1:p.Gly40AlafsTer?
NM_004364.4:c.161del NP_004355.2:p.Gly54AlafsTer?
NM_001287424.2:c.266del NP_001274353.1:p.Gly89AlafsTer?
NM_004364.5:c.161del MANE Select NP_004355.2:p.Gly54AlafsTer?
NM_001285829.2:c.-197del NP_001272758.1:n.-197del
NM_001287435.2:c.119del NP_001274364.1:p.Gly40AlafsTer?