Canonical Allele Identifier: CA2428298367

Gene: EBP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48527391_48527392delinsAG , CM000685.2:g.48527391_48527392delinsAG	GRCh38
NC_000023.10:g.48385779_48385780delinsAG , CM000685.1:g.48385779_48385780delinsAG	GRCh37
NC_000023.9:g.48270723_48270724delinsAG	NCBI36
NG_007452.1:g.10616_10617delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495186.6:c.469+106_469+107delinsAG MANE Select	ENSP00000417052.1:n.469+106_469+107delinsAG
ENST00000651615.1:c.469+106_469+107delinsAG	ENSP00000498524.1:n.469+106_469+107delinsAG
ENST00000276096.10:n.427+106_427+107delinsAG
ENST00000446158.5:c.469+106_469+107delinsAG	ENSP00000390031.1:n.469+106_469+107delinsAG
ENST00000466461.1:n.414_415delinsAG
ENST00000495186.5:c.469+106_469+107delinsAG	ENSP00000417052.1:n.469+106_469+107delinsAG
ENST00000498425.1:n.590+106_590+107delinsAG
NM_006579.2:c.469+106_469+107delinsAG	NP_006570.1:n.469+106_469+107delinsAG
NM_006579.3:c.469+106_469+107delinsAG MANE Select	NP_006570.1:n.469+106_469+107delinsAG