Canonical Allele Identifier: CA1772168850
Gene: EBF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26034436_26034437delinsGA , CM000670.2:g.26034436_26034437delinsGA GRCh38
NC_000008.10:g.25891952_25891953delinsGA , CM000670.1:g.25891952_25891953delinsGA GRCh37
NC_000008.9:g.25947869_25947870delinsGA NCBI36
NG_030344.1:g.15688_15689delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000520164.6:c.483-1284_483-1283delinsTC MANE Select ENSP00000430241.1:n.483-1284_483-1283delinsTC
ENST00000408929.7:c.39-1284_39-1283delinsTC ENSP00000386178.3:n.39-1284_39-1283delinsTC
ENST00000517825.1:n.802-1284_802-1283delinsTC
ENST00000520164.5:c.483-1284_483-1283delinsTC ENSP00000430241.1:n.483-1284_483-1283delinsTC
NM_022659.3:c.483-1284_483-1283delinsTC NP_073150.2:n.483-1284_483-1283delinsTC
NM_022659.4:c.483-1284_483-1283delinsTC MANE Select NP_073150.2:n.483-1284_483-1283delinsTC