Canonical Allele Identifier: CA506910011

Gene: CEBPA

Linked Data

• MyVariant Identifiers: chr19:g.33791149G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33300243G>T , CM000681.2:g.33300243G>T	GRCh38
NC_000019.9:g.33791149G>T , CM000681.1:g.33791149G>T	GRCh37
NC_000019.8:g.38482989G>T	NCBI36
NG_012022.1:g.7282C>A , LRG_456:g.7282C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.*1095C>A MANE Select	ENSP00000427514.1:n.*1095C>A
ENST00000498907.2:c.*1095C>A	ENSP00000427514.1:n.*1095C>A
NM_001285829.1:c.*1095C>A	NP_001272758.1:n.*1095C>A
NM_001287424.1:c.*1095C>A	NP_001274353.1:n.*1095C>A
NM_001287435.1:c.*1095C>A	NP_001274364.1:n.*1095C>A
NM_004364.4:c.*1095C>A	NP_004355.2:n.*1095C>A
NM_001287424.2:c.*1095C>A	NP_001274353.1:n.*1095C>A
NM_004364.5:c.*1095C>A MANE Select	NP_004355.2:n.*1095C>A
NM_001285829.2:c.*1095C>A	NP_001272758.1:n.*1095C>A
NM_001287435.2:c.*1095C>A	NP_001274364.1:n.*1095C>A