Canonical Allele Identifier: CA1425881519

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136687A= , CM000665.2:g.184136687A=	GRCh38
NC_000003.11:g.183854475A= , CM000665.1:g.183854475A=	GRCh37
NC_000003.10:g.185337169A=	NCBI36
NG_015826.1:g.6666A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432569.2:c.271A=	ENSP00000414775.1:p.Thr91=
ENST00000465218.3:n.294A=
ENST00000468748.7:n.254A=
ENST00000471832.2:c.*265A=	ENSP00000497786.1:n.*265A=
ENST00000484154.2:n.9A=
ENST00000491008.6:n.136A=
ENST00000492226.2:n.268A=
ENST00000492773.6:c.3A=
ENST00000647636.1:c.271A=	ENSP00000497505.1:p.Thr91=
ENST00000647909.1:c.271A=	ENSP00000498164.1:p.Thr91=
ENST00000648145.1:c.39A=
ENST00000648189.1:c.21A=
ENST00000648256.1:c.220A=	ENSP00000497356.1:p.Thr74=
ENST00000648314.1:c.271A=	ENSP00000496920.1:p.Thr91=
ENST00000648599.1:c.271A=	ENSP00000497159.1:p.Thr91=
ENST00000648630.1:c.265A=	ENSP00000497887.1:p.Thr89=
ENST00000648682.1:c.271A=	ENSP00000498185.1:p.Thr91=
ENST00000648882.1:c.*97A=	ENSP00000497603.1:n.*97A=
ENST00000648890.1:c.271A=	ENSP00000497503.1:p.Thr91=
ENST00000648915.2:c.271A= MANE Select	ENSP00000497160.1:p.Thr91=
ENST00000649545.1:c.5A=
ENST00000649688.1:c.271A=	ENSP00000497097.1:p.Thr91=
ENST00000649814.1:n.320A=
ENST00000650244.1:c.416A=	ENSP00000497227.1:n.416A=
ENST00000650270.1:c.138A=
ENST00000273783.7:c.271A=	ENSP00000273783.3:p.Thr91=
ENST00000432569.1:c.271A=	ENSP00000414775.1:p.Thr91=
ENST00000432982.5:c.245+12A=
ENST00000444495.1:c.271A=	ENSP00000409142.1:p.Thr91=
ENST00000471832.1:n.202A=
ENST00000481054.5:n.272A=
ENST00000491144.5:n.619A=
ENST00000498831.1:n.127A=
NM_003907.2:c.271A=	NP_003898.2:p.Thr91=
XR_924208.1:n.1222A=
NM_003907.3:c.271A= MANE Select	NP_003898.2:p.Thr91=
XM_011513266.3:c.-631A=	XP_011511568.1:n.-631A=
XR_001740352.2:n.634A=
XR_001740353.2:n.634A=
XR_924208.2:n.634A=