Canonical Allele Identifier: CA405274819

Gene: CEBPA

Linked Data

• gnomAD v4: 19-33301914-C-G
• MyVariant Identifiers: chr19:g.33792820C>G (hg19) ; chr19:g.33301914C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33301914C>G , CM000681.2:g.33301914C>G	GRCh38
NC_000019.9:g.33792820C>G , CM000681.1:g.33792820C>G	GRCh37
NC_000019.8:g.38484660C>G	NCBI36
NG_012022.1:g.5611G>C , LRG_456:g.5611G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.501G>C MANE Select	ENSP00000427514.1:p.Glu167Asp
ENST00000498907.2:c.501G>C	ENSP00000427514.1:p.Glu167Asp
NM_001285829.1:c.144G>C	NP_001272758.1:p.Glu48Asp
NM_001287424.1:c.606G>C	NP_001274353.1:p.Glu202Asp
NM_001287435.1:c.459G>C	NP_001274364.1:p.Glu153Asp
NM_004364.4:c.501G>C	NP_004355.2:p.Glu167Asp
NM_001287424.2:c.606G>C	NP_001274353.1:p.Glu202Asp
NM_004364.5:c.501G>C MANE Select	NP_004355.2:p.Glu167Asp
NM_001285829.2:c.144G>C	NP_001272758.1:p.Glu48Asp
NM_001287435.2:c.459G>C	NP_001274364.1:p.Glu153Asp