Canonical Allele Identifier: CA355386642

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183859724G>A (hg19) ; chr3:g.184141936G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184141936G>A , CM000665.2:g.184141936G>A	GRCh38
NC_000003.11:g.183859724G>A , CM000665.1:g.183859724G>A	GRCh37
NC_000003.10:g.185342418G>A	NCBI36
NG_015826.1:g.11915G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.1191G>A
ENST00000468748.7:n.1411G>A
ENST00000484154.2:n.1398G>A
ENST00000491008.6:n.1916G>A
ENST00000492226.2:n.1435G>A
ENST00000492773.6:c.922G>A
ENST00000647636.1:c.*17G>A	ENSP00000497505.1:n.*17G>A
ENST00000647909.1:c.1192G>A	ENSP00000498164.1:p.Val398Met
ENST00000648145.1:c.940G>A
ENST00000648189.1:c.986G>A
ENST00000648256.1:c.1140G>A	ENSP00000497356.1:n.1140G>A
ENST00000648314.1:c.*287G>A	ENSP00000496920.1:n.*287G>A
ENST00000648599.1:c.*451G>A	ENSP00000497159.1:n.*451G>A
ENST00000648630.1:c.1047G>A	ENSP00000497887.1:p.Trp349Ter
ENST00000648682.1:c.*8G>A	ENSP00000498185.1:n.*8G>A
ENST00000648882.1:c.*994G>A	ENSP00000497603.1:n.*994G>A
ENST00000648890.1:c.1168G>A	ENSP00000497503.1:p.Val390Met
ENST00000648915.2:c.1168G>A MANE Select	ENSP00000497160.1:p.Val390Met
ENST00000649545.1:c.589G>A
ENST00000649688.1:c.*461G>A	ENSP00000497097.1:n.*461G>A
ENST00000649814.1:n.1217G>A
ENST00000650270.1:c.1035G>A
ENST00000273783.7:c.1168G>A	ENSP00000273783.3:p.Val390Met
ENST00000432982.5:c.246-301G>A
ENST00000444495.1:c.1168G>A	ENSP00000409142.1:p.Val390Met
ENST00000479833.1:n.369G>A
ENST00000481054.5:n.1262G>A
ENST00000491144.5:n.1672G>A
ENST00000492773.5:n.51G>A
NM_003907.2:c.1168G>A	NP_003898.2:p.Val390Met
XM_011513265.1:c.418G>A	XP_011511567.1:p.Val140Met
XM_011513266.1:c.331G>A	XP_011511568.1:p.Val111Met
XR_924208.1:n.2119G>A
NM_003907.3:c.1168G>A MANE Select	NP_003898.2:p.Val390Met
XM_011513266.3:c.331G>A	XP_011511568.1:p.Val111Met
XR_001740352.2:n.1531G>A
XR_001740353.2:n.1531G>A
XR_924208.2:n.1531G>A