Canonical Allele Identifier: CA2581883753
Gene: EIF4E3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.71746592C>G , CM000665.2:g.71746592C>G GRCh38
NC_000003.11:g.71795743C>G , CM000665.1:g.71795743C>G GRCh37
NC_000003.10:g.71878433C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000647725.1:c.-959+7623G>C ENSP00000497585.1:n.-959+7623G>C
ENST00000295612.7:c.-291+6871G>C ENSP00000295612.3:n.-291+6871G>C
ENST00000421769.6:c.-291+8052G>C ENSP00000411762.2:n.-291+8052G>C
ENST00000448225.5:c.-291+7623G>C ENSP00000410350.1:n.-291+7623G>C
ENST00000496214.6:c.-291+7623G>C ENSP00000417889.2:n.-291+7623G>C
NM_001134649.2:c.-291+7623G>C NP_001128121.1:n.-291+7623G>C
NM_001282886.1:c.-291+6871G>C NP_001269815.1:n.-291+6871G>C
NM_173359.4:c.-291+8052G>C NP_775495.1:n.-291+8052G>C
XM_017006282.2:c.-341+7623G>C XP_016861771.1:n.-341+7623G>C
NM_001282886.2:c.-291+6871G>C NP_001269815.1:n.-291+6871G>C
NM_173359.5:c.-291+8052G>C NP_775495.1:n.-291+8052G>C
NM_001134649.3:c.-291+7623G>C NP_001128121.1:n.-291+7623G>C
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