Canonical Allele Identifier: CA2428298605
Gene: EBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528214_48528215delinsTC , CM000685.2:g.48528214_48528215delinsTC GRCh38
NC_000023.10:g.48386602_48386603delinsTC , CM000685.1:g.48386602_48386603delinsTC GRCh37
NC_000023.9:g.48271546_48271547delinsTC NCBI36
NG_007452.1:g.11439_11440delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.470-20_470-19delinsTC MANE Select ENSP00000417052.1:n.470-20_470-19delinsTC...
ENST00000651615.1:c.469+929_469+930delinsTC ENSP00000498524.1:n.469+929_469+930delins...
ENST00000276096.10:n.428-20_428-19delinsTC
ENST00000446158.5:c.470-20_470-19delinsTC ENSP00000390031.1:n.470-20_470-19delinsTC...
ENST00000495186.5:c.470-20_470-19delinsTC ENSP00000417052.1:n.470-20_470-19delinsTC...
ENST00000498425.1:n.591-20_591-19delinsTC
NM_006579.2:c.470-20_470-19delinsTC NP_006570.1:n.470-20_470-19delinsTC
NM_006579.3:c.470-20_470-19delinsTC MANE Select NP_006570.1:n.470-20_470-19delinsTC