Canonical Allele Identifier: CA2428298590
Gene: EBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48528188_48528189delinsTC , CM000685.2:g.48528188_48528189delinsTC GRCh38
NC_000023.10:g.48386576_48386577delinsTC , CM000685.1:g.48386576_48386577delinsTC GRCh37
NC_000023.9:g.48271520_48271521delinsTC NCBI36
NG_007452.1:g.11413_11414delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000495186.6:c.470-46_470-45delinsTC MANE Select ENSP00000417052.1:n.470-46_470-45delinsTC...
ENST00000651615.1:c.469+903_469+904delinsTC ENSP00000498524.1:n.469+903_469+904delins...
ENST00000276096.10:n.428-46_428-45delinsTC
ENST00000446158.5:c.470-46_470-45delinsTC ENSP00000390031.1:n.470-46_470-45delinsTC...
ENST00000495186.5:c.470-46_470-45delinsTC ENSP00000417052.1:n.470-46_470-45delinsTC...
ENST00000498425.1:n.591-46_591-45delinsTC
NM_006579.2:c.470-46_470-45delinsTC NP_006570.1:n.470-46_470-45delinsTC
NM_006579.3:c.470-46_470-45delinsTC MANE Select NP_006570.1:n.470-46_470-45delinsTC