Canonical Allele Identifier: CA2584317308

Gene: CEBPA

Linked Data

• gnomAD v4: 19-33300265-T-TCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33300265_33300266insCGG , CM000681.2:g.33300265_33300266insCGG	GRCh38
NC_000019.9:g.33791171_33791172insCGG , CM000681.1:g.33791171_33791172insCGG	GRCh37
NC_000019.8:g.38483011_38483012insCGG	NCBI36
NG_012022.1:g.7259_7260insCCG , LRG_456:g.7259_7260insCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.*1072_*1073insCCG MANE Select	ENSP00000427514.1:n.*1072_*1073insCCG
ENST00000498907.2:c.*1072_*1073insCCG	ENSP00000427514.1:n.*1072_*1073insCCG
NM_001285829.1:c.*1072_*1073insCCG	NP_001272758.1:n.*1072_*1073insCCG
NM_001287424.1:c.*1072_*1073insCCG	NP_001274353.1:n.*1072_*1073insCCG
NM_001287435.1:c.*1072_*1073insCCG	NP_001274364.1:n.*1072_*1073insCCG
NM_004364.4:c.*1072_*1073insCCG	NP_004355.2:n.*1072_*1073insCCG
NM_001287424.2:c.*1072_*1073insCCG	NP_001274353.1:n.*1072_*1073insCCG
NM_004364.5:c.*1072_*1073insCCG MANE Select	NP_004355.2:n.*1072_*1073insCCG
NM_001285829.2:c.*1072_*1073insCCG	NP_001272758.1:n.*1072_*1073insCCG
NM_001287435.2:c.*1072_*1073insCCG	NP_001274364.1:n.*1072_*1073insCCG