Canonical Allele Identifier: CA15291121

Gene: EIF4E3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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