Canonical Allele Identifier: CA2428297195
Gene: EBP HGNC NCBI

Linked Data

dbSNP Id: rs2061771352

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48523872dup , CM000685.2:g.48523872dup GRCh38
NC_000023.10:g.48382260dup , CM000685.1:g.48382260dup GRCh37
NC_000023.9:g.48267204dup NCBI36
NG_007452.1:g.7097dup

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.101dup MANE Select ENSP00000417052.1:p.Leu35ProfsTer?
ENST00000651615.1:c.101dup ENSP00000498524.1:p.Leu35ProfsTer?
ENST00000276096.10:n.110-51dup
ENST00000414061.1:c.101dup ENSP00000405832.1:p.Leu35ProfsTer?
ENST00000446158.5:c.101dup ENSP00000390031.1:p.Leu35ProfsTer?
ENST00000495186.5:c.101dup ENSP00000417052.1:p.Leu35ProfsTer?
ENST00000498425.1:n.222dup
NM_006579.2:c.101dup NP_006570.1:p.Leu35ProfsTer?
NM_006579.3:c.101dup MANE Select NP_006570.1:p.Leu35ProfsTer?