Canonical Allele Identifier: CA1425881421
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184136606_184136608delinsCTT , CM000665.2:g.184136606_184136608delinsCTT GRCh38
NC_000003.11:g.183854394_183854396delinsCTT , CM000665.1:g.183854394_183854396delinsCTT GRCh37
NC_000003.10:g.185337088_185337090delinsCTT NCBI36
NG_015826.1:g.6585_6587delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000432569.2:c.196-6_196-4delinsCTT ENSP00000414775.1:n.196-6_196-4delinsCTT
ENST00000465218.3:n.219-6_219-4delinsCTT
ENST00000468748.7:n.179-6_179-4delinsCTT
ENST00000471832.2:c.*190-6_*190-4delinsCTT ENSP00000497786.1:n.*190-6_*190-4delinsCTT
ENST00000491008.6:n.61-6_61-4delinsCTT
ENST00000492226.2:n.193-6_193-4delinsCTT
ENST00000647636.1:c.196-6_196-4delinsCTT ENSP00000497505.1:n.196-6_196-4delinsCTT
ENST00000647909.1:c.196-6_196-4delinsCTT ENSP00000498164.1:n.196-6_196-4delinsCTT
ENST00000648256.1:c.145-6_145-4delinsCTT ENSP00000497356.1:n.145-6_145-4delinsCTT
ENST00000648314.1:c.196-6_196-4delinsCTT ENSP00000496920.1:n.196-6_196-4delinsCTT
ENST00000648599.1:c.196-6_196-4delinsCTT ENSP00000497159.1:n.196-6_196-4delinsCTT
ENST00000648630.1:c.190-6_190-4delinsCTT ENSP00000497887.1:n.190-6_190-4delinsCTT
ENST00000648682.1:c.196-6_196-4delinsCTT ENSP00000498185.1:n.196-6_196-4delinsCTT
ENST00000648882.1:c.*22-6_*22-4delinsCTT ENSP00000497603.1:n.*22-6_*22-4delinsCTT
ENST00000648890.1:c.196-6_196-4delinsCTT ENSP00000497503.1:n.196-6_196-4delinsCTT
ENST00000648915.2:c.196-6_196-4delinsCTT MANE Select ENSP00000497160.1:n.196-6_196-4delinsCTT
ENST00000649688.1:c.196-6_196-4delinsCTT ENSP00000497097.1:n.196-6_196-4delinsCTT
ENST00000649814.1:n.245-6_245-4delinsCTT
ENST00000650244.1:c.341-6_341-4delinsCTT ENSP00000497227.1:n.341-6_341-4delinsCTT
ENST00000650270.1:c.63-6_63-4delinsCTT
ENST00000273783.7:c.196-6_196-4delinsCTT ENSP00000273783.3:n.196-6_196-4delinsCTT
ENST00000432569.1:c.196-6_196-4delinsCTT ENSP00000414775.1:n.196-6_196-4delinsCTT
ENST00000432982.5:c.182-6_182-4delinsCTT
ENST00000444495.1:c.196-6_196-4delinsCTT ENSP00000409142.1:n.196-6_196-4delinsCTT
ENST00000471832.1:n.127-6_127-4delinsCTT
ENST00000481054.5:n.197-6_197-4delinsCTT
ENST00000491144.5:n.544-6_544-4delinsCTT
ENST00000498831.1:n.52-6_52-4delinsCTT
NM_003907.2:c.196-6_196-4delinsCTT NP_003898.2:n.196-6_196-4delinsCTT
XR_924208.1:n.1147-6_1147-4delinsCTT
NM_003907.3:c.196-6_196-4delinsCTT MANE Select NP_003898.2:n.196-6_196-4delinsCTT
XM_011513266.3:c.-706-6_-706-4delinsCTT XP_011511568.1:n.-706-6_-706-4delinsCTT
XR_001740352.2:n.559-6_559-4delinsCTT
XR_001740353.2:n.559-6_559-4delinsCTT
XR_924208.2:n.559-6_559-4delinsCTT