Canonical Allele Identifier: CA1001217159

Gene: EIF2B3

Linked Data

• gnomAD v3: 1-44978619-TTC-T
• gnomAD v4: 1-44978619-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.44978621_44978622del , CM000663.2:g.44978621_44978622del	GRCh38
NC_000001.10:g.45444293_45444294del , CM000663.1:g.45444293_45444294del	GRCh37
NC_000001.9:g.45216880_45216881del	NCBI36
NG_015864.1:g.13069_13070del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360403.7:c.149-161_149-160del MANE Select	ENSP00000353575.2:n.149-161_149-160del
ENST00000360403.6:c.149-161_149-160del	ENSP00000353575.2:n.149-161_149-160del
ENST00000372182.6:n.262-161_262-160del
ENST00000372183.7:c.149-161_149-160del	ENSP00000361257.3:n.149-161_149-160del
ENST00000477953.5:n.252-161_252-160del
ENST00000480675.5:c.149-161_149-160del	ENSP00000485842.1:n.149-161_149-160del
ENST00000487532.5:n.261-161_261-160del
ENST00000497010.1:n.261-161_261-160del
ENST00000620860.4:c.149-161_149-160del	ENSP00000483996.1:n.149-161_149-160del
NM_001166588.2:c.149-161_149-160del	NP_001160060.1:n.149-161_149-160del
NM_001261418.1:c.149-161_149-160del	NP_001248347.1:n.149-161_149-160del
NM_020365.4:c.149-161_149-160del	NP_065098.1:n.149-161_149-160del
XM_011542396.1:c.149-161_149-160del	XP_011540698.1:n.149-161_149-160del
XM_017002745.2:c.149-161_149-160del	XP_016858234.1:n.149-161_149-160del
XM_017002746.1:c.-306-161_-306-160del	XP_016858235.1:n.-306-161_-306-160del
XM_017002747.1:c.-306-161_-306-160del	XP_016858236.1:n.-306-161_-306-160del
NM_020365.5:c.149-161_149-160del MANE Select	NP_065098.1:n.149-161_149-160del
NM_001166588.3:c.149-161_149-160del	NP_001160060.1:n.149-161_149-160del
NM_001261418.2:c.149-161_149-160del	NP_001248347.1:n.149-161_149-160del