Canonical Allele Identifier: CA995293356

Gene: CEBPA

Linked Data

• dbSNP Id: rs1967119937
• gnomAD v3: 19-33300260-TCA-T
• gnomAD v4: 19-33300260-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33300261_33300262del , CM000681.2:g.33300261_33300262del	GRCh38
NC_000019.9:g.33791167_33791168del , CM000681.1:g.33791167_33791168del	GRCh37
NC_000019.8:g.38483007_38483008del	NCBI36
NG_012022.1:g.7263_7264del , LRG_456:g.7263_7264del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.*1076_*1077del MANE Select	ENSP00000427514.1:n.*1076_*1077del
ENST00000498907.2:c.*1076_*1077del	ENSP00000427514.1:n.*1076_*1077del
NM_001285829.1:c.*1076_*1077del	NP_001272758.1:n.*1076_*1077del
NM_001287424.1:c.*1076_*1077del	NP_001274353.1:n.*1076_*1077del
NM_001287435.1:c.*1076_*1077del	NP_001274364.1:n.*1076_*1077del
NM_004364.4:c.*1076_*1077del	NP_004355.2:n.*1076_*1077del
NM_001287424.2:c.*1076_*1077del	NP_001274353.1:n.*1076_*1077del
NM_004364.5:c.*1076_*1077del MANE Select	NP_004355.2:n.*1076_*1077del
NM_001285829.2:c.*1076_*1077del	NP_001272758.1:n.*1076_*1077del
NM_001287435.2:c.*1076_*1077del	NP_001274364.1:n.*1076_*1077del