Canonical Allele Identifier: CA355381432

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183854400G>T (hg19) ; chr3:g.184136612G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136612G>T , CM000665.2:g.184136612G>T	GRCh38
NC_000003.11:g.183854400G>T , CM000665.1:g.183854400G>T	GRCh37
NC_000003.10:g.185337094G>T	NCBI36
NG_015826.1:g.6591G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432569.2:c.196G>T	ENSP00000414775.1:p.Val66Phe
ENST00000465218.3:n.219G>T
ENST00000468748.7:n.179G>T
ENST00000471832.2:c.*190G>T	ENSP00000497786.1:n.*190G>T
ENST00000491008.6:n.61G>T
ENST00000492226.2:n.193G>T
ENST00000647636.1:c.196G>T	ENSP00000497505.1:p.Val66Phe
ENST00000647909.1:c.196G>T	ENSP00000498164.1:p.Val66Phe
ENST00000648256.1:c.145G>T	ENSP00000497356.1:p.Val49Phe
ENST00000648314.1:c.196G>T	ENSP00000496920.1:p.Val66Phe
ENST00000648599.1:c.196G>T	ENSP00000497159.1:p.Val66Phe
ENST00000648630.1:c.190G>T	ENSP00000497887.1:p.Val64Phe
ENST00000648682.1:c.196G>T	ENSP00000498185.1:p.Val66Phe
ENST00000648882.1:c.*22G>T	ENSP00000497603.1:n.*22G>T
ENST00000648890.1:c.196G>T	ENSP00000497503.1:p.Val66Phe
ENST00000648915.2:c.196G>T MANE Select	ENSP00000497160.1:p.Val66Phe
ENST00000649688.1:c.196G>T	ENSP00000497097.1:p.Val66Phe
ENST00000649814.1:n.245G>T
ENST00000650244.1:c.341G>T	ENSP00000497227.1:n.341G>T
ENST00000650270.1:c.63G>T
ENST00000273783.7:c.196G>T	ENSP00000273783.3:p.Val66Phe
ENST00000432569.1:c.196G>T	ENSP00000414775.1:p.Val66Phe
ENST00000432982.5:c.182G>T
ENST00000444495.1:c.196G>T	ENSP00000409142.1:p.Val66Phe
ENST00000471832.1:n.127G>T
ENST00000481054.5:n.197G>T
ENST00000491144.5:n.544G>T
ENST00000498831.1:n.52G>T
NM_003907.2:c.196G>T	NP_003898.2:p.Val66Phe
XR_924208.1:n.1147G>T
NM_003907.3:c.196G>T MANE Select	NP_003898.2:p.Val66Phe
XM_011513266.3:c.-706G>T	XP_011511568.1:n.-706G>T
XR_001740352.2:n.559G>T
XR_001740353.2:n.559G>T
XR_924208.2:n.559G>T