Canonical Allele Identifier: CA507007748

Gene: CEBPA

Linked Data

• MyVariant Identifiers: chr19:g.33792823_33792824insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33301917_33301918insG , CM000681.2:g.33301917_33301918insG	GRCh38
NC_000019.9:g.33792823_33792824insG , CM000681.1:g.33792823_33792824insG	GRCh37
NC_000019.8:g.38484663_38484664insG	NCBI36
NG_012022.1:g.5607_5608insC , LRG_456:g.5607_5608insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000498907.3:c.497_498insC MANE Select	ENSP00000427514.1:p.Glu166AspfsTer4
ENST00000498907.2:c.497_498insC	ENSP00000427514.1:p.Glu166AspfsTer4
NM_001285829.1:c.140_141insC	NP_001272758.1:p.Glu47AspfsTer4
NM_001287424.1:c.602_603insC	NP_001274353.1:p.Glu201AspfsTer4
NM_001287435.1:c.455_456insC	NP_001274364.1:p.Glu152AspfsTer4
NM_004364.4:c.497_498insC	NP_004355.2:p.Glu166AspfsTer4
NM_001287424.2:c.602_603insC	NP_001274353.1:p.Glu201AspfsTer4
NM_004364.5:c.497_498insC MANE Select	NP_004355.2:p.Glu166AspfsTer4
NM_001285829.2:c.140_141insC	NP_001272758.1:p.Glu47AspfsTer4
NM_001287435.2:c.455_456insC	NP_001274364.1:p.Glu152AspfsTer4