Canonical Allele Identifier: CA405275051

Gene: CEBPA

Linked Data

• gnomAD v4: 19-33302023-T-C
• MyVariant Identifiers: chr19:g.33792929T>C (hg19) ; chr19:g.33302023T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33302023T>C , CM000681.2:g.33302023T>C	GRCh38
NC_000019.9:g.33792929T>C , CM000681.1:g.33792929T>C	GRCh37
NC_000019.8:g.38484769T>C	NCBI36
NG_012022.1:g.5502A>G , LRG_456:g.5502A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.392A>G MANE Select	ENSP00000427514.1:p.Tyr131Cys
ENST00000498907.2:c.392A>G	ENSP00000427514.1:p.Tyr131Cys
NM_001285829.1:c.35A>G	NP_001272758.1:p.Tyr12Cys
NM_001287424.1:c.497A>G	NP_001274353.1:p.Tyr166Cys
NM_001287435.1:c.350A>G	NP_001274364.1:p.Tyr117Cys
NM_004364.4:c.392A>G	NP_004355.2:p.Tyr131Cys
NM_001287424.2:c.497A>G	NP_001274353.1:p.Tyr166Cys
NM_004364.5:c.392A>G MANE Select	NP_004355.2:p.Tyr131Cys
NM_001285829.2:c.35A>G	NP_001272758.1:p.Tyr12Cys
NM_001287435.2:c.350A>G	NP_001274364.1:p.Tyr117Cys