Canonical Allele Identifier: CA405275257
Gene: CEBPA HGNC NCBI

Linked Data

dbSNP Id: rs2145263252

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33302123T>G , CM000681.2:g.33302123T>G GRCh38
NC_000019.9:g.33793029T>G , CM000681.1:g.33793029T>G GRCh37
NC_000019.8:g.38484869T>G NCBI36
NG_012022.1:g.5402A>C , LRG_456:g.5402A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.292A>C MANE Select ENSP00000427514.1:p.Thr98Pro
ENST00000498907.2:c.292A>C ENSP00000427514.1:p.Thr98Pro
NM_001285829.1:c.-66A>C NP_001272758.1:n.-66A>C
NM_001287424.1:c.397A>C NP_001274353.1:p.Thr133Pro
NM_001287435.1:c.250A>C NP_001274364.1:p.Thr84Pro
NM_004364.4:c.292A>C NP_004355.2:p.Thr98Pro
NM_001287424.2:c.397A>C NP_001274353.1:p.Thr133Pro
NM_004364.5:c.292A>C MANE Select NP_004355.2:p.Thr98Pro
NM_001285829.2:c.-66A>C NP_001272758.1:n.-66A>C
NM_001287435.2:c.250A>C NP_001274364.1:p.Thr84Pro