Canonical Allele Identifier: CA522559908
Gene: EIF2B3 HGNC NCBI

Linked Data

dbSNP Id: rs1279979615

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.44978640_44978641insC , CM000663.2:g.44978640_44978641insC GRCh38
NC_000001.10:g.45444312_45444313insC , CM000663.1:g.45444312_45444313insC GRCh37
NC_000001.9:g.45216899_45216900insC NCBI36
NG_015864.1:g.13049_13050insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000360403.7:c.149-181_149-180insG MANE Select ENSP00000353575.2:n.149-181_149-180insG
ENST00000360403.6:c.149-181_149-180insG ENSP00000353575.2:n.149-181_149-180insG
ENST00000372182.6:n.262-181_262-180insG
ENST00000372183.7:c.149-181_149-180insG ENSP00000361257.3:n.149-181_149-180insG
ENST00000477953.5:n.252-181_252-180insG
ENST00000480675.5:c.149-181_149-180insG ENSP00000485842.1:n.149-181_149-180insG
ENST00000487532.5:n.261-181_261-180insG
ENST00000497010.1:n.261-181_261-180insG
ENST00000620860.4:c.149-181_149-180insG ENSP00000483996.1:n.149-181_149-180insG
NM_001166588.2:c.149-181_149-180insG NP_001160060.1:n.149-181_149-180insG
NM_001261418.1:c.149-181_149-180insG NP_001248347.1:n.149-181_149-180insG
NM_020365.4:c.149-181_149-180insG NP_065098.1:n.149-181_149-180insG
XM_011542396.1:c.149-181_149-180insG XP_011540698.1:n.149-181_149-180insG
XM_017002745.2:c.149-181_149-180insG XP_016858234.1:n.149-181_149-180insG
XM_017002746.1:c.-306-181_-306-180insG XP_016858235.1:n.-306-181_-306-180insG
XM_017002747.1:c.-306-181_-306-180insG XP_016858236.1:n.-306-181_-306-180insG
NM_020365.5:c.149-181_149-180insG MANE Select NP_065098.1:n.149-181_149-180insG
NM_001166588.3:c.149-181_149-180insG NP_001160060.1:n.149-181_149-180insG
NM_001261418.2:c.149-181_149-180insG NP_001248347.1:n.149-181_149-180insG