Canonical Allele Identifier: CA2428298318
Gene: EBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48527276_48527278delinsGTC , CM000685.2:g.48527276_48527278delinsGTC GRCh38
NC_000023.10:g.48385664_48385666delinsGTC , CM000685.1:g.48385664_48385666delinsGTC GRCh37
NC_000023.9:g.48270608_48270610delinsGTC NCBI36
NG_007452.1:g.10501_10503delinsGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000495186.6:c.460_462delinsGTC MANE Select ENSP00000417052.1:p.Val154=
ENST00000651615.1:c.460_462delinsGTC ENSP00000498524.1:p.Val154=
ENST00000276096.10:n.418_420delinsGTC
ENST00000446158.5:c.460_462delinsGTC ENSP00000390031.1:p.Val154=
ENST00000466461.1:n.299_301delinsGTC
ENST00000495186.5:c.460_462delinsGTC ENSP00000417052.1:p.Val154=
ENST00000498425.1:n.581_583delinsGTC
NM_006579.2:c.460_462delinsGTC NP_006570.1:p.Val154=
NM_006579.3:c.460_462delinsGTC MANE Select NP_006570.1:p.Val154=
Search 100 bp 5'
Search 100 bp 3'