Canonical Allele Identifier: CA355382071

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855578C>T (hg19) ; chr3:g.184137790C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137790C>T , CM000665.2:g.184137790C>T	GRCh38
NC_000003.11:g.183855578C>T , CM000665.1:g.183855578C>T	GRCh37
NC_000003.10:g.185338272C>T	NCBI36
NG_015826.1:g.7769C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.514C>T
ENST00000468748.7:n.474C>T
ENST00000484154.2:n.1112C>T
ENST00000491008.6:n.1239C>T
ENST00000492226.2:n.488C>T
ENST00000492773.6:c.223C>T
ENST00000647636.1:c.491C>T	ENSP00000497505.1:p.Ala164Val
ENST00000647909.1:c.491C>T	ENSP00000498164.1:p.Ala164Val
ENST00000648145.1:c.259C>T
ENST00000648189.1:c.241C>T
ENST00000648256.1:c.440C>T	ENSP00000497356.1:p.Ala147Val
ENST00000648314.1:c.491C>T	ENSP00000496920.1:p.Ala164Val
ENST00000648599.1:c.491C>T	ENSP00000497159.1:p.Ala164Val
ENST00000648630.1:c.485C>T	ENSP00000497887.1:p.Ala162Val
ENST00000648682.1:c.491C>T	ENSP00000498185.1:p.Ala164Val
ENST00000648882.1:c.*317C>T	ENSP00000497603.1:n.*317C>T
ENST00000648890.1:c.491C>T	ENSP00000497503.1:p.Ala164Val
ENST00000648915.2:c.491C>T MANE Select	ENSP00000497160.1:p.Ala164Val
ENST00000649545.1:c.225C>T
ENST00000649688.1:c.491C>T	ENSP00000497097.1:p.Ala164Val
ENST00000649814.1:n.540C>T
ENST00000650244.1:c.636C>T	ENSP00000497227.1:n.636C>T
ENST00000650270.1:c.358C>T
ENST00000273783.7:c.491C>T	ENSP00000273783.3:p.Ala164Val
ENST00000432982.5:c.245+1115C>T
ENST00000444495.1:c.491C>T	ENSP00000409142.1:p.Ala164Val
ENST00000481054.5:n.492C>T
ENST00000491008.5:n.455C>T
ENST00000491144.5:n.839C>T
ENST00000498831.1:n.446C>T
NM_003907.2:c.491C>T	NP_003898.2:p.Ala164Val
XR_924208.1:n.1442C>T
NM_003907.3:c.491C>T MANE Select	NP_003898.2:p.Ala164Val
XM_011513266.3:c.-411C>T	XP_011511568.1:n.-411C>T
XR_001740352.2:n.854C>T
XR_001740353.2:n.854C>T
XR_924208.2:n.854C>T