Canonical Allele Identifier: CA506909872

Gene: CEBPA

Linked Data

• MyVariant Identifiers: chr19:g.33791102A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33300196A>C , CM000681.2:g.33300196A>C	GRCh38
NC_000019.9:g.33791102A>C , CM000681.1:g.33791102A>C	GRCh37
NC_000019.8:g.38482942A>C	NCBI36
NG_012022.1:g.7329T>G , LRG_456:g.7329T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.*1142T>G MANE Select	ENSP00000427514.1:n.*1142T>G
ENST00000498907.2:c.*1142T>G	ENSP00000427514.1:n.*1142T>G
NM_001285829.1:c.*1142T>G	NP_001272758.1:n.*1142T>G
NM_001287424.1:c.*1142T>G	NP_001274353.1:n.*1142T>G
NM_001287435.1:c.*1142T>G	NP_001274364.1:n.*1142T>G
NM_004364.4:c.*1142T>G	NP_004355.2:n.*1142T>G
NM_001287424.2:c.*1142T>G	NP_001274353.1:n.*1142T>G
NM_004364.5:c.*1142T>G MANE Select	NP_004355.2:n.*1142T>G
NM_001285829.2:c.*1142T>G	NP_001272758.1:n.*1142T>G
NM_001287435.2:c.*1142T>G	NP_001274364.1:n.*1142T>G