Canonical Allele Identifier: CA2584317317

Gene: CEBPA

Linked Data

• gnomAD v4: 19-33300282-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33300282_33300283insTT , CM000681.2:g.33300282_33300283insTT	GRCh38
NC_000019.9:g.33791188_33791189insTT , CM000681.1:g.33791188_33791189insTT	GRCh37
NC_000019.8:g.38483028_38483029insTT	NCBI36
NG_012022.1:g.7242_7243insAA , LRG_456:g.7242_7243insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.*1055_*1056insAA MANE Select	ENSP00000427514.1:n.*1055_*1056insAA
ENST00000498907.2:c.*1055_*1056insAA	ENSP00000427514.1:n.*1055_*1056insAA
NM_001285829.1:c.*1055_*1056insAA	NP_001272758.1:n.*1055_*1056insAA
NM_001287424.1:c.*1055_*1056insAA	NP_001274353.1:n.*1055_*1056insAA
NM_001287435.1:c.*1055_*1056insAA	NP_001274364.1:n.*1055_*1056insAA
NM_004364.4:c.*1055_*1056insAA	NP_004355.2:n.*1055_*1056insAA
NM_001287424.2:c.*1055_*1056insAA	NP_001274353.1:n.*1055_*1056insAA
NM_004364.5:c.*1055_*1056insAA MANE Select	NP_004355.2:n.*1055_*1056insAA
NM_001285829.2:c.*1055_*1056insAA	NP_001272758.1:n.*1055_*1056insAA
NM_001287435.2:c.*1055_*1056insAA	NP_001274364.1:n.*1055_*1056insAA