Canonical Allele Identifier: CA2428298601
Gene: EBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528208_48528211delinsTCTC , CM000685.2:g.48528208_48528211delinsTCTC GRCh38
NC_000023.10:g.48386596_48386599delinsTCTC , CM000685.1:g.48386596_48386599delinsTCTC GRCh37
NC_000023.9:g.48271540_48271543delinsTCTC NCBI36
NG_007452.1:g.11433_11436delinsTCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.470-26_470-23delinsTCTC MANE Select ENSP00000417052.1:n.470-26_470-23delinsTC...
ENST00000651615.1:c.469+923_469+926delinsTCTC ENSP00000498524.1:n.469+923_469+926delins...
ENST00000276096.10:n.428-26_428-23delinsTCTC
ENST00000446158.5:c.470-26_470-23delinsTCTC ENSP00000390031.1:n.470-26_470-23delinsTC...
ENST00000495186.5:c.470-26_470-23delinsTCTC ENSP00000417052.1:n.470-26_470-23delinsTC...
ENST00000498425.1:n.591-26_591-23delinsTCTC
NM_006579.2:c.470-26_470-23delinsTCTC NP_006570.1:n.470-26_470-23delinsTCTC
NM_006579.3:c.470-26_470-23delinsTCTC MANE Select NP_006570.1:n.470-26_470-23delinsTCTC