Canonical Allele Identifier: CA2584317296

Gene: CEBPA

Linked Data

• gnomAD v4: 19-33300252-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33300252_33300253insAA , CM000681.2:g.33300252_33300253insAA	GRCh38
NC_000019.9:g.33791158_33791159insAA , CM000681.1:g.33791158_33791159insAA	GRCh37
NC_000019.8:g.38482998_38482999insAA	NCBI36
NG_012022.1:g.7272_7273insTT , LRG_456:g.7272_7273insTT

Transcript Alleles

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