Canonical Allele Identifier: CA2526944187

Gene: CEBPA

Linked Data

• gnomAD v4: 19-33300408-AATATTTGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33300410_33300417del , CM000681.2:g.33300410_33300417del	GRCh38
NC_000019.9:g.33791316_33791323del , CM000681.1:g.33791316_33791323del	GRCh37
NC_000019.8:g.38483156_38483163del	NCBI36
NG_012022.1:g.7109_7116del , LRG_456:g.7109_7116del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.*922_*929del MANE Select	ENSP00000427514.1:n.*922_*929del
ENST00000498907.2:c.*922_*929del	ENSP00000427514.1:n.*922_*929del
NM_001285829.1:c.*922_*929del	NP_001272758.1:n.*922_*929del
NM_001287424.1:c.*922_*929del	NP_001274353.1:n.*922_*929del
NM_001287435.1:c.*922_*929del	NP_001274364.1:n.*922_*929del
NM_004364.4:c.*922_*929del	NP_004355.2:n.*922_*929del
NM_001287424.2:c.*922_*929del	NP_001274353.1:n.*922_*929del
NM_004364.5:c.*922_*929del MANE Select	NP_004355.2:n.*922_*929del
NM_001285829.2:c.*922_*929del	NP_001272758.1:n.*922_*929del
NM_001287435.2:c.*922_*929del	NP_001274364.1:n.*922_*929del