Canonical Allele Identifier: CA437323548
Gene: EIF2B5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183855740G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137952G>A , CM000665.2:g.184137952G>A GRCh38
NC_000003.11:g.183855740G>A , CM000665.1:g.183855740G>A GRCh37
NC_000003.10:g.185338434G>A NCBI36
NG_015826.1:g.7931G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.584G>A
ENST00000468748.7:n.544G>A
ENST00000484154.2:n.1182G>A
ENST00000491008.6:n.1309G>A
ENST00000492226.2:n.558G>A
ENST00000492773.6:c.293G>A
ENST00000647636.1:c.561G>A ENSP00000497505.1:p.Glu187=
ENST00000647909.1:c.585G>A ENSP00000498164.1:p.Glu195=
ENST00000648145.1:c.329G>A
ENST00000648189.1:c.311G>A
ENST00000648256.1:c.510G>A ENSP00000497356.1:p.Glu170=
ENST00000648314.1:c.561G>A ENSP00000496920.1:p.Glu187=
ENST00000648599.1:c.561G>A ENSP00000497159.1:p.Glu187=
ENST00000648630.1:c.555G>A ENSP00000497887.1:p.Glu185=
ENST00000648682.1:c.561G>A ENSP00000498185.1:p.Glu187=
ENST00000648882.1:c.*387G>A ENSP00000497603.1:n.*387G>A
ENST00000648890.1:c.561G>A ENSP00000497503.1:p.Glu187=
ENST00000648915.2:c.561G>A MANE Select ENSP00000497160.1:p.Glu187=
ENST00000649545.1:c.295G>A
ENST00000649688.1:c.561G>A ENSP00000497097.1:p.Glu187=
ENST00000649814.1:n.610G>A
ENST00000650270.1:c.428G>A
ENST00000273783.7:c.561G>A ENSP00000273783.3:p.Glu187=
ENST00000432982.5:c.245+1277G>A
ENST00000444495.1:c.561G>A ENSP00000409142.1:p.Glu187=
ENST00000468748.5:n.14G>A
ENST00000481054.5:n.562G>A
ENST00000491008.5:n.525G>A
ENST00000491144.5:n.1001G>A
ENST00000498831.1:n.516G>A
NM_003907.2:c.561G>A NP_003898.2:p.Glu187=
XR_924208.1:n.1512G>A
NM_003907.3:c.561G>A MANE Select NP_003898.2:p.Glu187=
XM_011513266.3:c.-341G>A XP_011511568.1:n.-341G>A
XR_001740352.2:n.924G>A
XR_001740353.2:n.924G>A
XR_924208.2:n.924G>A