Canonical Allele Identifier: CA1335326653
Gene: EIF4E2 HGNC NCBI

Linked Data

dbSNP Id: rs1692730585

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232561724_232561728del , CM000664.2:g.232561724_232561728del GRCh38
NC_000002.11:g.233426434_233426438del , CM000664.1:g.233426434_233426438del GRCh37
NC_000002.10:g.233134678_233134682del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000409167.8:c.136-2523_136-2519del ENSP00000387328.3:n.136-2523_136-2519del
ENST00000409495.6:c.271-2523_271-2519del ENSP00000386876.1:n.271-2523_271-2519del
ENST00000687222.1:c.136-2523_136-2519del ENSP00000508671.1:n.136-2523_136-2519del
ENST00000690794.1:c.-30-2523_-30-2519del ENSP00000509248.1:n.-30-2523_-30-2519del
ENST00000258416.8:c.271-2523_271-2519del MANE Select ENSP00000258416.3:n.271-2523_271-2519del
ENST00000258416.7:c.271-2523_271-2519del ENSP00000258416.3:n.271-2523_271-2519del
ENST00000409098.5:c.271-2523_271-2519del ENSP00000386996.1:n.271-2523_271-2519del
ENST00000409167.7:c.136-2523_136-2519del ENSP00000387328.3:n.136-2523_136-2519del
ENST00000409322.5:c.136-2523_136-2519del ENSP00000386424.1:n.136-2523_136-2519del
ENST00000409394.5:c.136-2523_136-2519del ENSP00000386983.1:n.136-2523_136-2519del
ENST00000409495.5:c.271-2523_271-2519del ENSP00000386876.1:n.271-2523_271-2519del
ENST00000409514.5:c.271-2523_271-2519del ENSP00000387336.1:n.271-2523_271-2519del
ENST00000454501.1:c.256-2523_256-2519del ENSP00000390904.1:n.256-2523_256-2519del
NM_001276336.1:c.271-2523_271-2519del NP_001263265.1:n.271-2523_271-2519del
NM_001276337.1:c.136-2523_136-2519del NP_001263266.1:n.136-2523_136-2519del
NM_001282958.1:c.271-2523_271-2519del NP_001269887.1:n.271-2523_271-2519del
NM_004846.3:c.271-2523_271-2519del NP_004837.1:n.271-2523_271-2519del
XM_005246975.2:c.136-2523_136-2519del XP_005247032.1:n.136-2523_136-2519del
XM_011512206.1:c.256-2523_256-2519del XP_011510508.1:n.256-2523_256-2519del
NM_001330201.1:c.136-2523_136-2519del NP_001317130.1:n.136-2523_136-2519del
NM_001330202.1:c.256-2523_256-2519del NP_001317131.1:n.256-2523_256-2519del
NM_001330203.1:c.136-2523_136-2519del NP_001317132.1:n.136-2523_136-2519del
NM_004846.4:c.271-2523_271-2519del MANE Select NP_004837.1:n.271-2523_271-2519del
NM_001276336.2:c.271-2523_271-2519del NP_001263265.1:n.271-2523_271-2519del
NM_001276337.2:c.136-2523_136-2519del NP_001263266.1:n.136-2523_136-2519del
NM_001282958.2:c.271-2523_271-2519del NP_001269887.1:n.271-2523_271-2519del
NM_001330201.2:c.136-2523_136-2519del NP_001317130.1:n.136-2523_136-2519del
NM_001330202.2:c.256-2523_256-2519del NP_001317131.1:n.256-2523_256-2519del
NM_001330203.2:c.136-2523_136-2519del NP_001317132.1:n.136-2523_136-2519del