Canonical Allele Identifier: CA2814183453

Gene: CEBPA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33300252_33300253insAT , CM000681.2:g.33300252_33300253insAT	GRCh38
NC_000019.9:g.33791158_33791159insAT , CM000681.1:g.33791158_33791159insAT	GRCh37
NC_000019.8:g.38482998_38482999insAT	NCBI36
NG_012022.1:g.7272_7273insAT , LRG_456:g.7272_7273insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.*1085_*1086insAT MANE Select	ENSP00000427514.1:n.*1085_*1086insAT
ENST00000498907.2:c.*1085_*1086insAT	ENSP00000427514.1:n.*1085_*1086insAT
NM_001285829.1:c.*1085_*1086insAT	NP_001272758.1:n.*1085_*1086insAT
NM_001287424.1:c.*1085_*1086insAT	NP_001274353.1:n.*1085_*1086insAT
NM_001287435.1:c.*1085_*1086insAT	NP_001274364.1:n.*1085_*1086insAT
NM_004364.4:c.*1085_*1086insAT	NP_004355.2:n.*1085_*1086insAT
NM_001287424.2:c.*1085_*1086insAT	NP_001274353.1:n.*1085_*1086insAT
NM_004364.5:c.*1085_*1086insAT MANE Select	NP_004355.2:n.*1085_*1086insAT
NM_001285829.2:c.*1085_*1086insAT	NP_001272758.1:n.*1085_*1086insAT
NM_001287435.2:c.*1085_*1086insAT	NP_001274364.1:n.*1085_*1086insAT