Canonical Allele Identifier: CA2428298370

Gene: EBP

Linked Data

• dbSNP Id: rs2061782675

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48527397_48527400dup , CM000685.2:g.48527397_48527400dup	GRCh38
NC_000023.10:g.48385785_48385788dup , CM000685.1:g.48385785_48385788dup	GRCh37
NC_000023.9:g.48270729_48270732dup	NCBI36
NG_007452.1:g.10622_10625dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495186.6:c.469+112_469+115dup MANE Select	ENSP00000417052.1:n.469+112_469+115dup
ENST00000651615.1:c.469+112_469+115dup	ENSP00000498524.1:n.469+112_469+115dup
ENST00000276096.10:n.427+112_427+115dup
ENST00000446158.5:c.469+112_469+115dup	ENSP00000390031.1:n.469+112_469+115dup
ENST00000466461.1:n.420_423dup
ENST00000495186.5:c.469+112_469+115dup	ENSP00000417052.1:n.469+112_469+115dup
ENST00000498425.1:n.590+112_590+115dup
NM_006579.2:c.469+112_469+115dup	NP_006570.1:n.469+112_469+115dup
NM_006579.3:c.469+112_469+115dup MANE Select	NP_006570.1:n.469+112_469+115dup