Canonical Allele Identifier: CA507007341

Gene: CEBPA

Linked Data

• MyVariant Identifiers: chr19:g.33793030_33793031insC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33302124_33302125insC , CM000681.2:g.33302124_33302125insC	GRCh38
NC_000019.9:g.33793030_33793031insC , CM000681.1:g.33793030_33793031insC	GRCh37
NC_000019.8:g.38484870_38484871insC	NCBI36
NG_012022.1:g.5400_5401insG , LRG_456:g.5400_5401insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.290_291insG MANE Select	ENSP00000427514.1:p.Thr98HisfsTer10
ENST00000498907.2:c.290_291insG	ENSP00000427514.1:p.Thr98HisfsTer10
NM_001285829.1:c.-68_-67insG	NP_001272758.1:n.-68_-67insG
NM_001287424.1:c.395_396insG	NP_001274353.1:p.Thr133HisfsTer10
NM_001287435.1:c.248_249insG	NP_001274364.1:p.Thr84HisfsTer10
NM_004364.4:c.290_291insG	NP_004355.2:p.Thr98HisfsTer10
NM_001287424.2:c.395_396insG	NP_001274353.1:p.Thr133HisfsTer10
NM_004364.5:c.290_291insG MANE Select	NP_004355.2:p.Thr98HisfsTer10
NM_001285829.2:c.-68_-67insG	NP_001272758.1:n.-68_-67insG
NM_001287435.2:c.248_249insG	NP_001274364.1:p.Thr84HisfsTer10