Canonical Allele Identifier: CA437323486
Gene: EIF2B5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183855698G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137910G>A , CM000665.2:g.184137910G>A GRCh38
NC_000003.11:g.183855698G>A , CM000665.1:g.183855698G>A GRCh37
NC_000003.10:g.185338392G>A NCBI36
NG_015826.1:g.7889G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.542G>A
ENST00000468748.7:n.502G>A
ENST00000484154.2:n.1140G>A
ENST00000491008.6:n.1267G>A
ENST00000492226.2:n.516G>A
ENST00000492773.6:c.251G>A
ENST00000647636.1:c.519G>A ENSP00000497505.1:p.Lys173=
ENST00000647909.1:c.543G>A ENSP00000498164.1:p.Lys181=
ENST00000648145.1:c.287G>A
ENST00000648189.1:c.269G>A
ENST00000648256.1:c.468G>A ENSP00000497356.1:p.Lys156=
ENST00000648314.1:c.519G>A ENSP00000496920.1:p.Lys173=
ENST00000648599.1:c.519G>A ENSP00000497159.1:p.Lys173=
ENST00000648630.1:c.513G>A ENSP00000497887.1:p.Lys171=
ENST00000648682.1:c.519G>A ENSP00000498185.1:p.Lys173=
ENST00000648882.1:c.*345G>A ENSP00000497603.1:n.*345G>A
ENST00000648890.1:c.519G>A ENSP00000497503.1:p.Lys173=
ENST00000648915.2:c.519G>A MANE Select ENSP00000497160.1:p.Lys173=
ENST00000649545.1:c.253G>A
ENST00000649688.1:c.519G>A ENSP00000497097.1:p.Lys173=
ENST00000649814.1:n.568G>A
ENST00000650244.1:c.664G>A ENSP00000497227.1:n.664G>A
ENST00000650270.1:c.386G>A
ENST00000273783.7:c.519G>A ENSP00000273783.3:p.Lys173=
ENST00000432982.5:c.245+1235G>A
ENST00000444495.1:c.519G>A ENSP00000409142.1:p.Lys173=
ENST00000481054.5:n.520G>A
ENST00000491008.5:n.483G>A
ENST00000491144.5:n.959G>A
ENST00000498831.1:n.474G>A
NM_003907.2:c.519G>A NP_003898.2:p.Lys173=
XR_924208.1:n.1470G>A
NM_003907.3:c.519G>A MANE Select NP_003898.2:p.Lys173=
XM_011513266.3:c.-383G>A XP_011511568.1:n.-383G>A
XR_001740352.2:n.882G>A
XR_001740353.2:n.882G>A
XR_924208.2:n.882G>A