Canonical Allele Identifier: CA1001217125
Gene: EIF2B3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.44978617_44978618insTTTTTTTT , CM000663.2:g.44978617_44978618insTTTTTTTT GRCh38
NC_000001.10:g.45444289_45444290insTTTTTTTT , CM000663.1:g.45444289_45444290insTTTTTTTT GRCh37
NC_000001.9:g.45216876_45216877insTTTTTTTT NCBI36
NG_015864.1:g.13072_13073insAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000360403.7:c.149-158_149-157insAAAAAAAA MANE Select ENSP00000353575.2:n.149-158_149-157insAAAAAAAA
ENST00000360403.6:c.149-158_149-157insAAAAAAAA ENSP00000353575.2:n.149-158_149-157insAAAAAAAA
ENST00000372182.6:n.262-158_262-157insAAAAAAAA
ENST00000372183.7:c.149-158_149-157insAAAAAAAA ENSP00000361257.3:n.149-158_149-157insAAAAAAAA
ENST00000477953.5:n.252-158_252-157insAAAAAAAA
ENST00000480675.5:c.149-158_149-157insAAAAAAAA ENSP00000485842.1:n.149-158_149-157insAAAAAAAA
ENST00000487532.5:n.261-158_261-157insAAAAAAAA
ENST00000497010.1:n.261-158_261-157insAAAAAAAA
ENST00000620860.4:c.149-158_149-157insAAAAAAAA ENSP00000483996.1:n.149-158_149-157insAAAAAAAA
NM_001166588.2:c.149-158_149-157insAAAAAAAA NP_001160060.1:n.149-158_149-157insAAAAAAAA
NM_001261418.1:c.149-158_149-157insAAAAAAAA NP_001248347.1:n.149-158_149-157insAAAAAAAA
NM_020365.4:c.149-158_149-157insAAAAAAAA NP_065098.1:n.149-158_149-157insAAAAAAAA
XM_011542396.1:c.149-158_149-157insAAAAAAAA XP_011540698.1:n.149-158_149-157insAAAAAAAA
XM_017002745.2:c.149-158_149-157insAAAAAAAA XP_016858234.1:n.149-158_149-157insAAAAAAAA
XM_017002746.1:c.-306-158_-306-157insAAAAAAAA XP_016858235.1:n.-306-158_-306-157insAAAAAAAA
XM_017002747.1:c.-306-158_-306-157insAAAAAAAA XP_016858236.1:n.-306-158_-306-157insAAAAAAAA
NM_020365.5:c.149-158_149-157insAAAAAAAA MANE Select NP_065098.1:n.149-158_149-157insAAAAAAAA
NM_001166588.3:c.149-158_149-157insAAAAAAAA NP_001160060.1:n.149-158_149-157insAAAAAAAA
NM_001261418.2:c.149-158_149-157insAAAAAAAA NP_001248347.1:n.149-158_149-157insAAAAAAAA