Canonical Allele Identifier: CA507007839

Gene: CEBPA

Linked Data

• MyVariant Identifiers: chr19:g.33792931G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33302025G>C , CM000681.2:g.33302025G>C	GRCh38
NC_000019.9:g.33792931G>C , CM000681.1:g.33792931G>C	GRCh37
NC_000019.8:g.38484771G>C	NCBI36
NG_012022.1:g.5500C>G , LRG_456:g.5500C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000498907.3:c.390C>G MANE Select	ENSP00000427514.1:p.Gly130=
ENST00000498907.2:c.390C>G	ENSP00000427514.1:p.Gly130=
NM_001285829.1:c.33C>G	NP_001272758.1:p.Gly11=
NM_001287424.1:c.495C>G	NP_001274353.1:p.Gly165=
NM_001287435.1:c.348C>G	NP_001274364.1:p.Gly116=
NM_004364.4:c.390C>G	NP_004355.2:p.Gly130=
NM_001287424.2:c.495C>G	NP_001274353.1:p.Gly165=
NM_004364.5:c.390C>G MANE Select	NP_004355.2:p.Gly130=
NM_001285829.2:c.33C>G	NP_001272758.1:p.Gly11=
NM_001287435.2:c.348C>G	NP_001274364.1:p.Gly116=