Canonical Allele Identifier: CA845315964

Gene: EIF3E

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.108215779A>T , CM000670.2:g.108215779A>T	GRCh38
NC_000008.10:g.109228008A>T , CM000670.1:g.109228008A>T	GRCh37
NC_000008.9:g.109297184A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220849.10:c.951+633T>A MANE Select	ENSP00000220849.5:n.951+633T>A
ENST00000518100.6:c.*1048+633T>A	ENSP00000429327.1:n.*1048+633T>A
ENST00000518345.2:c.804+633T>A	ENSP00000430678.2:n.804+633T>A
ENST00000519030.6:c.672+633T>A	ENSP00000428796.1:n.672+633T>A
ENST00000519627.2:c.570+633T>A	ENSP00000430839.2:n.570+633T>A
ENST00000521297.2:c.723-12276T>A	ENSP00000429968.2:n.723-12276T>A
ENST00000521614.6:n.2317+633T>A
ENST00000522352.6:c.-22-12276T>A	ENSP00000428170.2:n.-22-12276T>A
ENST00000522445.6:c.*746+633T>A	ENSP00000430709.1:n.*746+633T>A
ENST00000523674.2:n.968+633T>A
ENST00000676530.1:n.4264+633T>A
ENST00000676642.1:c.*487+633T>A	ENSP00000503038.1:n.*487+633T>A
ENST00000676663.1:c.672+633T>A	ENSP00000504047.1:n.672+633T>A
ENST00000676698.1:c.951+633T>A	ENSP00000503133.1:n.951+633T>A
ENST00000676706.1:c.*580+633T>A	ENSP00000503667.1:n.*580+633T>A
ENST00000676892.1:c.951+633T>A	ENSP00000503531.1:n.951+633T>A
ENST00000677040.1:c.804+633T>A	ENSP00000504521.1:n.804+633T>A
ENST00000677084.1:c.672+633T>A	ENSP00000504517.1:n.672+633T>A
ENST00000677272.1:c.864+633T>A	ENSP00000504529.1:n.864+633T>A
ENST00000677317.1:n.690+633T>A
ENST00000677409.1:c.804+633T>A	ENSP00000504815.1:n.804+633T>A
ENST00000677501.1:n.1231+633T>A
ENST00000677524.1:n.681+633T>A
ENST00000677590.1:n.923+633T>A
ENST00000677614.1:c.981+633T>A	ENSP00000504788.1:n.981+633T>A
ENST00000677674.1:c.1032+633T>A	ENSP00000503434.1:n.1032+633T>A
ENST00000677696.1:n.1715+633T>A
ENST00000677965.1:n.7460+633T>A
ENST00000678004.1:c.*566+633T>A	ENSP00000503071.1:n.*566+633T>A
ENST00000678023.1:c.981+633T>A	ENSP00000502937.1:n.981+633T>A
ENST00000678042.1:c.951+633T>A	ENSP00000503596.1:n.951+633T>A
ENST00000678243.1:c.723-12276T>A	ENSP00000503845.1:n.723-12276T>A
ENST00000678334.1:c.981+633T>A	ENSP00000503856.1:n.981+633T>A
ENST00000678773.1:c.618+633T>A	ENSP00000504386.1:n.618+633T>A
ENST00000678797.1:c.981+633T>A	ENSP00000504851.1:n.981+633T>A
ENST00000678881.1:c.804+633T>A	ENSP00000504404.1:n.804+633T>A
ENST00000678901.1:c.951+633T>A	ENSP00000502918.1:n.951+633T>A
ENST00000678937.1:c.672+633T>A	ENSP00000503965.1:n.672+633T>A
ENST00000679198.1:c.672+633T>A	ENSP00000503334.1:n.672+633T>A
ENST00000220849.9:c.951+633T>A	ENSP00000220849.5:n.951+633T>A
ENST00000519030.5:c.672+633T>A	ENSP00000428796.1:n.672+633T>A
ENST00000519517.5:n.582+633T>A
ENST00000519627.1:c.570+633T>A	ENSP00000430839.1:n.570+633T>A
ENST00000521614.5:n.1583+633T>A
ENST00000522352.5:c.193-12276T>A
NM_001568.2:c.951+633T>A	NP_001559.1:n.951+633T>A
XM_017013398.2:c.951+633T>A	XP_016868887.2:n.951+633T>A
NM_001568.3:c.951+633T>A MANE Select	NP_001559.1:n.951+633T>A