Canonical Allele Identifier: CA342017
Gene: CEBPA HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 21397
ClinVar RCV Id: RCV000020583
dbSNP Id: rs137852731

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33302215_33302218dup , CM000681.2:g.33302215_33302218dup GRCh38
NC_000019.9:g.33793121_33793124dup , CM000681.1:g.33793121_33793124dup GRCh37
NC_000019.8:g.38484961_38484964dup NCBI36
NG_012022.1:g.5308_5311dup , LRG_456:g.5308_5311dup

Transcript Alleles

HGVS Amino-acid change
NM_001285829.1:c.-160_-157dup VV NP_001272758.1:p.=
NM_001287424.1:c.303_306dup VV NP_001274353.1:p.Ile103LeufsTer?
NM_001287435.1:c.156_159dup VV NP_001274364.1:p.Ile54LeufsTer?
NM_004364.4:c.198_201dup VV NP_004355.2:p.Ile68LeufsTer?
ENST00000498907.2:c.198_201dup ENSP00000427514.1:p.Ile68LeufsTer?