Canonical Allele Identifier: CA2695234249
Gene: EBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48523781_48523791del , CM000685.2:g.48523781_48523791del GRCh38
NC_000023.10:g.48382169_48382179del , CM000685.1:g.48382169_48382179del GRCh37
NC_000023.9:g.48267113_48267123del NCBI36
NG_007452.1:g.7006_7016del

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.10_20del MANE Select ENSP00000417052.1:p.Asn4LeufsTer17
ENST00000651615.1:c.10_20del ENSP00000498524.1:p.Asn4LeufsTer17
ENST00000276096.10:n.110-142_110-132del
ENST00000414061.1:c.10_20del ENSP00000405832.1:p.Asn4LeufsTer17
ENST00000446158.5:c.10_20del ENSP00000390031.1:p.Asn4LeufsTer17
ENST00000495186.5:c.10_20del ENSP00000417052.1:p.Asn4LeufsTer17
ENST00000498425.1:n.131_141del
NM_006579.2:c.10_20del NP_006570.1:p.Asn4LeufsTer17
NM_006579.3:c.10_20del MANE Select NP_006570.1:p.Asn4LeufsTer17
Search 100 bp 5'
Search 100 bp 3'