Canonical Allele Identifier: CA2473570422
Gene: EIF2B3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.44978614_44978615delinsAT , CM000663.2:g.44978614_44978615delinsAT GRCh38
NC_000001.10:g.45444286_45444287delinsAT , CM000663.1:g.45444286_45444287delinsAT GRCh37
NC_000001.9:g.45216873_45216874delinsAT NCBI36
NG_015864.1:g.13075_13076delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360403.7:c.149-155_149-154delinsAT MANE Select ENSP00000353575.2:n.149-155_149-154delinsAT
ENST00000360403.6:c.149-155_149-154delinsAT ENSP00000353575.2:n.149-155_149-154delinsAT
ENST00000372182.6:n.262-155_262-154delinsAT
ENST00000372183.7:c.149-155_149-154delinsAT ENSP00000361257.3:n.149-155_149-154delinsAT
ENST00000477953.5:n.252-155_252-154delinsAT
ENST00000480675.5:c.149-155_149-154delinsAT ENSP00000485842.1:n.149-155_149-154delinsAT
ENST00000487532.5:n.261-155_261-154delinsAT
ENST00000497010.1:n.261-155_261-154delinsAT
ENST00000620860.4:c.149-155_149-154delinsAT ENSP00000483996.1:n.149-155_149-154delinsAT
NM_001166588.2:c.149-155_149-154delinsAT NP_001160060.1:n.149-155_149-154delinsAT
NM_001261418.1:c.149-155_149-154delinsAT NP_001248347.1:n.149-155_149-154delinsAT
NM_020365.4:c.149-155_149-154delinsAT NP_065098.1:n.149-155_149-154delinsAT
XM_011542396.1:c.149-155_149-154delinsAT XP_011540698.1:n.149-155_149-154delinsAT
XM_017002745.2:c.149-155_149-154delinsAT XP_016858234.1:n.149-155_149-154delinsAT
XM_017002746.1:c.-306-155_-306-154delinsAT XP_016858235.1:n.-306-155_-306-154delinsAT
XM_017002747.1:c.-306-155_-306-154delinsAT XP_016858236.1:n.-306-155_-306-154delinsAT
NM_020365.5:c.149-155_149-154delinsAT MANE Select NP_065098.1:n.149-155_149-154delinsAT
NM_001166588.3:c.149-155_149-154delinsAT NP_001160060.1:n.149-155_149-154delinsAT
NM_001261418.2:c.149-155_149-154delinsAT NP_001248347.1:n.149-155_149-154delinsAT