Canonical Allele Identifier: CA437323368

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855477A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137689A>T , CM000665.2:g.184137689A>T	GRCh38
NC_000003.11:g.183855477A>T , CM000665.1:g.183855477A>T	GRCh37
NC_000003.10:g.185338171A>T	NCBI36
NG_015826.1:g.7668A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000465218.3:n.413A>T
ENST00000468748.7:n.373A>T
ENST00000484154.2:n.1011A>T
ENST00000491008.6:n.1138A>T
ENST00000492226.2:n.387A>T
ENST00000492773.6:c.122A>T
ENST00000647636.1:c.390A>T	ENSP00000497505.1:p.Ser130=
ENST00000647909.1:c.390A>T	ENSP00000498164.1:p.Ser130=
ENST00000648145.1:c.158A>T
ENST00000648189.1:c.140A>T
ENST00000648256.1:c.339A>T	ENSP00000497356.1:p.Ser113=
ENST00000648314.1:c.390A>T	ENSP00000496920.1:p.Ser130=
ENST00000648599.1:c.390A>T	ENSP00000497159.1:p.Ser130=
ENST00000648630.1:c.384A>T	ENSP00000497887.1:p.Ser128=
ENST00000648682.1:c.390A>T	ENSP00000498185.1:p.Ser130=
ENST00000648882.1:c.*216A>T	ENSP00000497603.1:n.*216A>T
ENST00000648890.1:c.390A>T	ENSP00000497503.1:p.Ser130=
ENST00000648915.2:c.390A>T MANE Select	ENSP00000497160.1:p.Ser130=
ENST00000649545.1:c.124A>T
ENST00000649688.1:c.390A>T	ENSP00000497097.1:p.Ser130=
ENST00000649814.1:n.439A>T
ENST00000650244.1:c.535A>T	ENSP00000497227.1:n.535A>T
ENST00000650270.1:c.257A>T
ENST00000273783.7:c.390A>T	ENSP00000273783.3:p.Ser130=
ENST00000432982.5:c.245+1014A>T
ENST00000444495.1:c.390A>T	ENSP00000409142.1:p.Ser130=
ENST00000481054.5:n.391A>T
ENST00000491008.5:n.354A>T
ENST00000491144.5:n.738A>T
ENST00000498831.1:n.345A>T
NM_003907.2:c.390A>T	NP_003898.2:p.Ser130=
XR_924208.1:n.1341A>T
NM_003907.3:c.390A>T MANE Select	NP_003898.2:p.Ser130=
XM_011513266.3:c.-512A>T	XP_011511568.1:n.-512A>T
XR_001740352.2:n.753A>T
XR_001740353.2:n.753A>T
XR_924208.2:n.753A>T