Canonical Allele Identifier: CA1001217337
Gene: EIF2B3 HGNC NCBI

Linked Data

dbSNP Id: rs1644480327

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.44978653_44978654insTTTTTCT , CM000663.2:g.44978653_44978654insTTTTTCT GRCh38
NC_000001.10:g.45444325_45444326insTTTTTCT , CM000663.1:g.45444325_45444326insTTTTTCT GRCh37
NC_000001.9:g.45216912_45216913insTTTTTCT NCBI36
NG_015864.1:g.13037_13038insGAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000360403.7:c.149-193_149-192insGAAAAAA MANE Select ENSP00000353575.2:n.149-193_149-192insGAAAAAA
ENST00000360403.6:c.149-193_149-192insGAAAAAA ENSP00000353575.2:n.149-193_149-192insGAAAAAA
ENST00000372182.6:n.262-193_262-192insGAAAAAA
ENST00000372183.7:c.149-193_149-192insGAAAAAA ENSP00000361257.3:n.149-193_149-192insGAAAAAA
ENST00000477953.5:n.252-193_252-192insGAAAAAA
ENST00000480675.5:c.149-193_149-192insGAAAAAA ENSP00000485842.1:n.149-193_149-192insGAAAAAA
ENST00000487532.5:n.261-193_261-192insGAAAAAA
ENST00000497010.1:n.261-193_261-192insGAAAAAA
ENST00000620860.4:c.149-193_149-192insGAAAAAA ENSP00000483996.1:n.149-193_149-192insGAAAAAA
NM_001166588.2:c.149-193_149-192insGAAAAAA NP_001160060.1:n.149-193_149-192insGAAAAAA
NM_001261418.1:c.149-193_149-192insGAAAAAA NP_001248347.1:n.149-193_149-192insGAAAAAA
NM_020365.4:c.149-193_149-192insGAAAAAA NP_065098.1:n.149-193_149-192insGAAAAAA
XM_011542396.1:c.149-193_149-192insGAAAAAA XP_011540698.1:n.149-193_149-192insGAAAAAA
XM_017002745.2:c.149-193_149-192insGAAAAAA XP_016858234.1:n.149-193_149-192insGAAAAAA
XM_017002746.1:c.-306-193_-306-192insGAAAAAA XP_016858235.1:n.-306-193_-306-192insGAAAAAA
XM_017002747.1:c.-306-193_-306-192insGAAAAAA XP_016858236.1:n.-306-193_-306-192insGAAAAAA
NM_020365.5:c.149-193_149-192insGAAAAAA MANE Select NP_065098.1:n.149-193_149-192insGAAAAAA
NM_001166588.3:c.149-193_149-192insGAAAAAA NP_001160060.1:n.149-193_149-192insGAAAAAA
NM_001261418.2:c.149-193_149-192insGAAAAAA NP_001248347.1:n.149-193_149-192insGAAAAAA