Canonical Allele Identifier: CA2428297160
Gene: EBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48523765_48523767delinsCAA , CM000685.2:g.48523765_48523767delinsCAA GRCh38
NC_000023.10:g.48382153_48382155delinsCAA , CM000685.1:g.48382153_48382155delinsCAA GRCh37
NC_000023.9:g.48267097_48267099delinsCAA NCBI36
NG_007452.1:g.6990_6992delinsCAA

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.-7_-5delinsCAA MANE Select ENSP00000417052.1:n.-7_-5delinsCAA
ENST00000651615.1:c.-7_-5delinsCAA ENSP00000498524.1:n.-7_-5delinsCAA
ENST00000276096.10:n.110-158_110-156delinsCAA
ENST00000414061.1:c.-7_-5delinsCAA ENSP00000405832.1:n.-7_-5delinsCAA
ENST00000446158.5:c.-7_-5delinsCAA ENSP00000390031.1:n.-7_-5delinsCAA
ENST00000495186.5:c.-7_-5delinsCAA ENSP00000417052.1:n.-7_-5delinsCAA
ENST00000498425.1:n.115_117delinsCAA
NM_006579.2:c.-7_-5delinsCAA NP_006570.1:n.-7_-5delinsCAA
NM_006579.3:c.-7_-5delinsCAA MANE Select NP_006570.1:n.-7_-5delinsCAA