Canonical Allele Identifier: CA437146675

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183856004G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138216G>T , CM000665.2:g.184138216G>T	GRCh38
NC_000003.11:g.183856004G>T , CM000665.1:g.183856004G>T	GRCh37
NC_000003.10:g.185338698G>T	NCBI36
NG_015826.1:g.8195G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.758G>T
ENST00000468748.7:n.718G>T
ENST00000484154.2:n.1356G>T
ENST00000491008.6:n.1483G>T
ENST00000492226.2:n.732G>T
ENST00000492773.6:c.489G>T
ENST00000647636.1:c.735G>T	ENSP00000497505.1:p.Leu245=
ENST00000647909.1:c.759G>T	ENSP00000498164.1:p.Leu253=
ENST00000648145.1:c.503G>T
ENST00000648189.1:c.485G>T
ENST00000648256.1:c.684G>T	ENSP00000497356.1:p.Leu228=
ENST00000648314.1:c.735G>T	ENSP00000496920.1:p.Leu245=
ENST00000648599.1:c.735G>T	ENSP00000497159.1:p.Leu245=
ENST00000648630.1:c.729G>T	ENSP00000497887.1:p.Leu243=
ENST00000648682.1:c.735G>T	ENSP00000498185.1:p.Leu245=
ENST00000648882.1:c.*561G>T	ENSP00000497603.1:n.*561G>T
ENST00000648890.1:c.735G>T	ENSP00000497503.1:p.Leu245=
ENST00000648915.2:c.735G>T MANE Select	ENSP00000497160.1:p.Leu245=
ENST00000649545.1:c.469G>T
ENST00000649688.1:c.735G>T	ENSP00000497097.1:p.Leu245=
ENST00000649814.1:n.784G>T
ENST00000650270.1:c.602G>T
ENST00000273783.7:c.735G>T	ENSP00000273783.3:p.Leu245=
ENST00000432982.5:c.245+1541G>T
ENST00000444495.1:c.735G>T	ENSP00000409142.1:p.Leu245=
ENST00000468748.5:n.188G>T
ENST00000479833.1:n.51G>T
ENST00000481054.5:n.736G>T
ENST00000491008.5:n.699G>T
ENST00000491144.5:n.1175G>T
NM_003907.2:c.735G>T	NP_003898.2:p.Leu245=
XR_924208.1:n.1686G>T
NM_003907.3:c.735G>T MANE Select	NP_003898.2:p.Leu245=
XM_011513266.3:c.-167G>T	XP_011511568.1:n.-167G>T
XR_001740352.2:n.1098G>T
XR_001740353.2:n.1098G>T
XR_924208.2:n.1098G>T