Canonical Allele Identifier: CA1425885694
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184140520C= , CM000665.2:g.184140520C= GRCh38
NC_000003.11:g.183858308C= , CM000665.1:g.183858308C= GRCh37
NC_000003.10:g.185341002C= NCBI36
NG_015826.1:g.10499C=

Transcript Alleles

HGVS Amino-acid change
ENST00000465218.3:n.969C=
ENST00000468748.7:n.1189C=
ENST00000484154.2:n.1387-1405C=
ENST00000491008.6:n.1694C=
ENST00000492226.2:n.1203C=
ENST00000492773.6:c.700C=
ENST00000647636.1:c.946C= ENSP00000497505.1:p.Arg316=
ENST00000647909.1:c.970C= ENSP00000498164.1:p.Arg324=
ENST00000648145.1:c.714C=
ENST00000648189.1:c.760C=
ENST00000648256.1:c.918C= ENSP00000497356.1:n.918C=
ENST00000648314.1:c.*65C= ENSP00000496920.1:n.*65C=
ENST00000648599.1:c.*229C= ENSP00000497159.1:n.*229C=
ENST00000648630.1:c.940C= ENSP00000497887.1:p.Arg314=
ENST00000648682.1:c.946C= ENSP00000498185.1:p.Arg316=
ENST00000648882.1:c.*772C= ENSP00000497603.1:n.*772C=
ENST00000648890.1:c.946C= ENSP00000497503.1:p.Arg316=
ENST00000648915.2:c.946C= MANE Select ENSP00000497160.1:p.Arg316=
ENST00000649545.1:c.577+363C=
ENST00000649688.1:c.*229C= ENSP00000497097.1:n.*229C=
ENST00000649814.1:n.995C=
ENST00000650270.1:c.813C=
ENST00000273783.7:c.946C= ENSP00000273783.3:p.Arg316=
ENST00000432982.5:c.246-1717C=
ENST00000444495.1:c.946C= ENSP00000409142.1:p.Arg316=
ENST00000468748.5:n.659C=
ENST00000479833.1:n.262C=
ENST00000481054.5:n.1040C=
ENST00000491144.5:n.1450C=
ENST00000493740.1:n.176C=
NM_003907.2:c.946C= NP_003898.2:p.Arg316=
XM_011513265.1:c.196C= XP_011511567.1:p.Arg66=
XM_011513266.1:c.109C= XP_011511568.1:p.Arg37=
XR_924208.1:n.1897C=
NM_003907.3:c.946C= MANE Select NP_003898.2:p.Arg316=
XM_011513266.3:c.109C= XP_011511568.1:p.Arg37=
XR_001740352.2:n.1309C=
XR_001740353.2:n.1309C=
XR_924208.2:n.1309C=