Canonical Allele Identifier: CA1001217155
Gene: EIF2B3 HGNC NCBI

Linked Data

dbSNP Id: rs1330964091

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.44978620_44978621insTTT , CM000663.2:g.44978620_44978621insTTT GRCh38
NC_000001.10:g.45444292_45444293insTTT , CM000663.1:g.45444292_45444293insTTT GRCh37
NC_000001.9:g.45216879_45216880insTTT NCBI36
NG_015864.1:g.13071_13072insAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000360403.7:c.149-159_149-158insAAA MANE Select ENSP00000353575.2:n.149-159_149-158insAAA
ENST00000360403.6:c.149-159_149-158insAAA ENSP00000353575.2:n.149-159_149-158insAAA
ENST00000372182.6:n.262-159_262-158insAAA
ENST00000372183.7:c.149-159_149-158insAAA ENSP00000361257.3:n.149-159_149-158insAAA
ENST00000477953.5:n.252-159_252-158insAAA
ENST00000480675.5:c.149-159_149-158insAAA ENSP00000485842.1:n.149-159_149-158insAAA
ENST00000487532.5:n.261-159_261-158insAAA
ENST00000497010.1:n.261-159_261-158insAAA
ENST00000620860.4:c.149-159_149-158insAAA ENSP00000483996.1:n.149-159_149-158insAAA
NM_001166588.2:c.149-159_149-158insAAA NP_001160060.1:n.149-159_149-158insAAA
NM_001261418.1:c.149-159_149-158insAAA NP_001248347.1:n.149-159_149-158insAAA
NM_020365.4:c.149-159_149-158insAAA NP_065098.1:n.149-159_149-158insAAA
XM_011542396.1:c.149-159_149-158insAAA XP_011540698.1:n.149-159_149-158insAAA
XM_017002745.2:c.149-159_149-158insAAA XP_016858234.1:n.149-159_149-158insAAA
XM_017002746.1:c.-306-159_-306-158insAAA XP_016858235.1:n.-306-159_-306-158insAAA
XM_017002747.1:c.-306-159_-306-158insAAA XP_016858236.1:n.-306-159_-306-158insAAA
NM_020365.5:c.149-159_149-158insAAA MANE Select NP_065098.1:n.149-159_149-158insAAA
NM_001166588.3:c.149-159_149-158insAAA NP_001160060.1:n.149-159_149-158insAAA
NM_001261418.2:c.149-159_149-158insAAA NP_001248347.1:n.149-159_149-158insAAA