Canonical Allele Identifier: CA2332659500
Gene: CEBPA HGNC NCBI

Linked Data

dbSNP Id: rs1967122765

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33300370_33300371dup , CM000681.2:g.33300370_33300371dup GRCh38
NC_000019.9:g.33791276_33791277dup , CM000681.1:g.33791276_33791277dup GRCh37
NC_000019.8:g.38483116_38483117dup NCBI36
NG_012022.1:g.7156_7157dup , LRG_456:g.7156_7157dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.*969_*970dup MANE Select ENSP00000427514.1:n.*969_*970dup
ENST00000498907.2:c.*969_*970dup ENSP00000427514.1:n.*969_*970dup
NM_001285829.1:c.*969_*970dup NP_001272758.1:n.*969_*970dup
NM_001287424.1:c.*969_*970dup NP_001274353.1:n.*969_*970dup
NM_001287435.1:c.*969_*970dup NP_001274364.1:n.*969_*970dup
NM_004364.4:c.*969_*970dup NP_004355.2:n.*969_*970dup
NM_001287424.2:c.*969_*970dup NP_001274353.1:n.*969_*970dup
NM_004364.5:c.*969_*970dup MANE Select NP_004355.2:n.*969_*970dup
NM_001285829.2:c.*969_*970dup NP_001272758.1:n.*969_*970dup
NM_001287435.2:c.*969_*970dup NP_001274364.1:n.*969_*970dup