Canonical Allele Identifier: CA21761661

Gene: EIF2B3

Linked Data

• dbSNP Id: rs563059806
• gnomAD v2: 1-45444276-C-CATTCCCCCAAT
• gnomAD v3: 1-44978604-C-CATTCCCCCAAT
• gnomAD v4: 1-44978604-C-CATTCCCCCAAT
• MyVariant Identifiers: chr1:g.45444276_45444277insATTCCCCCAAT (hg19) ; chr1:g.44978604_44978605insATTCCCCCAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.44978606_44978616dup , CM000663.2:g.44978606_44978616dup	GRCh38
NC_000001.10:g.45444278_45444288dup , CM000663.1:g.45444278_45444288dup	GRCh37
NC_000001.9:g.45216865_45216875dup	NCBI36
NG_015864.1:g.13075_13085dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360403.7:c.149-155_149-145dup MANE Select	ENSP00000353575.2:n.149-155_149-145dup
ENST00000360403.6:c.149-155_149-145dup	ENSP00000353575.2:n.149-155_149-145dup
ENST00000372182.6:n.262-155_262-145dup
ENST00000372183.7:c.149-155_149-145dup	ENSP00000361257.3:n.149-155_149-145dup
ENST00000477953.5:n.252-155_252-145dup
ENST00000480675.5:c.149-155_149-145dup	ENSP00000485842.1:n.149-155_149-145dup
ENST00000487532.5:n.261-155_261-145dup
ENST00000497010.1:n.261-155_261-145dup
ENST00000620860.4:c.149-155_149-145dup	ENSP00000483996.1:n.149-155_149-145dup
NM_001166588.2:c.149-155_149-145dup	NP_001160060.1:n.149-155_149-145dup
NM_001261418.1:c.149-155_149-145dup	NP_001248347.1:n.149-155_149-145dup
NM_020365.4:c.149-155_149-145dup	NP_065098.1:n.149-155_149-145dup
XM_011542396.1:c.149-155_149-145dup	XP_011540698.1:n.149-155_149-145dup
XM_017002745.2:c.149-155_149-145dup	XP_016858234.1:n.149-155_149-145dup
XM_017002746.1:c.-306-155_-306-145dup	XP_016858235.1:n.-306-155_-306-145dup
XM_017002747.1:c.-306-155_-306-145dup	XP_016858236.1:n.-306-155_-306-145dup
NM_020365.5:c.149-155_149-145dup MANE Select	NP_065098.1:n.149-155_149-145dup
NM_001166588.3:c.149-155_149-145dup	NP_001160060.1:n.149-155_149-145dup
NM_001261418.2:c.149-155_149-145dup	NP_001248347.1:n.149-155_149-145dup