Canonical Allele Identifier: CA1140664561

Gene: EIF2B3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.44978622_44978653delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000663.2:g.44978622_44978653delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000001.10:g.45444294_45444325delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000663.1:g.45444294_45444325delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000001.9:g.45216881_45216912delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_015864.1:g.13037_13068delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360403.7:c.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA MANE Select	ENSP00000353575.2:n.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAA...
ENST00000360403.6:c.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000353575.2:n.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAA...
ENST00000372182.6:n.262-193_262-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ENST00000372183.7:c.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000361257.3:n.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAA...
ENST00000477953.5:n.252-193_252-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ENST00000480675.5:c.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000485842.1:n.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAA...
ENST00000487532.5:n.261-193_261-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ENST00000497010.1:n.261-193_261-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ENST00000620860.4:c.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000483996.1:n.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAA...
NM_001166588.2:c.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_001160060.1:n.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAA...
NM_001261418.1:c.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_001248347.1:n.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAA...
NM_020365.4:c.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_065098.1:n.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAA...
XM_011542396.1:c.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XP_011540698.1:n.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAA...
XM_017002745.2:c.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XP_016858234.1:n.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAA...
XM_017002746.1:c.-306-193_-306-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XP_016858235.1:n.-306-193_-306-162delinsAAAAAAAAAAAAAAAAAAAAA...
XM_017002747.1:c.-306-193_-306-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XP_016858236.1:n.-306-193_-306-162delinsAAAAAAAAAAAAAAAAAAAAA...
NM_020365.5:c.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA MANE Select	NP_065098.1:n.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAA...
NM_001166588.3:c.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_001160060.1:n.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAA...
NM_001261418.2:c.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_001248347.1:n.149-193_149-162delinsAAAAAAAAAAAAAAAAAAAAAAA...