Canonical Allele Identifier: CA1772168897
Gene: EBF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26034465_26034469delinsCAACA , CM000670.2:g.26034465_26034469delinsCAACA GRCh38
NC_000008.10:g.25891981_25891985delinsCAACA , CM000670.1:g.25891981_25891985delinsCAACA GRCh37
NC_000008.9:g.25947898_25947902delinsCAACA NCBI36
NG_030344.1:g.15656_15660delinsTGTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000520164.6:c.483-1316_483-1312delinsTGTTG MANE Select ENSP00000430241.1:n.483-1316_483-1312delinsTGTTG
ENST00000408929.7:c.39-1316_39-1312delinsTGTTG ENSP00000386178.3:n.39-1316_39-1312delinsTGTTG
ENST00000517825.1:n.802-1316_802-1312delinsTGTTG
ENST00000520164.5:c.483-1316_483-1312delinsTGTTG ENSP00000430241.1:n.483-1316_483-1312delinsTGTTG
NM_022659.3:c.483-1316_483-1312delinsTGTTG NP_073150.2:n.483-1316_483-1312delinsTGTTG
NM_022659.4:c.483-1316_483-1312delinsTGTTG MANE Select NP_073150.2:n.483-1316_483-1312delinsTGTTG