Canonical Allele Identifier: CA1425887149
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184141985C= , CM000665.2:g.184141985C= GRCh38
NC_000003.11:g.183859773C= , CM000665.1:g.183859773C= GRCh37
NC_000003.10:g.185342467C= NCBI36
NG_015826.1:g.11964C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.1240C=
ENST00000468748.7:n.1460C=
ENST00000484154.2:n.1447C=
ENST00000491008.6:n.1965C=
ENST00000492226.2:n.1484C=
ENST00000492773.6:c.971C=
ENST00000647636.1:c.*66C= ENSP00000497505.1:n.*66C=
ENST00000647909.1:c.1241C= ENSP00000498164.1:p.Ala414=
ENST00000648145.1:c.989C=
ENST00000648189.1:c.1035C=
ENST00000648256.1:c.1189C= ENSP00000497356.1:n.1189C=
ENST00000648314.1:c.*336C= ENSP00000496920.1:n.*336C=
ENST00000648599.1:c.*500C= ENSP00000497159.1:n.*500C=
ENST00000648630.1:c.1096C= ENSP00000497887.1:p.His366=
ENST00000648682.1:c.*57C= ENSP00000498185.1:n.*57C=
ENST00000648882.1:c.*1043C= ENSP00000497603.1:n.*1043C=
ENST00000648890.1:c.1217C= ENSP00000497503.1:p.Ala406=
ENST00000648915.2:c.1217C= MANE Select ENSP00000497160.1:p.Ala406=
ENST00000649545.1:c.638C=
ENST00000649688.1:c.*510C= ENSP00000497097.1:n.*510C=
ENST00000649814.1:n.1266C=
ENST00000650270.1:c.1084C=
ENST00000273783.7:c.1217C= ENSP00000273783.3:p.Ala406=
ENST00000432982.5:c.246-252C=
ENST00000444495.1:c.1217C= ENSP00000409142.1:p.Ala406=
ENST00000479833.1:n.418C=
ENST00000481054.5:n.1311C=
ENST00000491144.5:n.1721C=
ENST00000492773.5:n.100C=
NM_003907.2:c.1217C= NP_003898.2:p.Ala406=
XM_011513265.1:c.467C= XP_011511567.1:p.Ala156=
XM_011513266.1:c.380C= XP_011511568.1:p.Ala127=
XR_924208.1:n.2168C=
NM_003907.3:c.1217C= MANE Select NP_003898.2:p.Ala406=
XM_011513266.3:c.380C= XP_011511568.1:p.Ala127=
XR_001740352.2:n.1580C=
XR_001740353.2:n.1580C=
XR_924208.2:n.1580C=