Canonical Allele Identifier: CA355381446

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183854408G>C (hg19) ; chr3:g.184136620G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136620G>C , CM000665.2:g.184136620G>C	GRCh38
NC_000003.11:g.183854408G>C , CM000665.1:g.183854408G>C	GRCh37
NC_000003.10:g.185337102G>C	NCBI36
NG_015826.1:g.6599G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432569.2:c.204G>C	ENSP00000414775.1:p.Leu68Phe
ENST00000465218.3:n.227G>C
ENST00000468748.7:n.187G>C
ENST00000471832.2:c.*198G>C	ENSP00000497786.1:n.*198G>C
ENST00000491008.6:n.69G>C
ENST00000492226.2:n.201G>C
ENST00000647636.1:c.204G>C	ENSP00000497505.1:p.Leu68Phe
ENST00000647909.1:c.204G>C	ENSP00000498164.1:p.Leu68Phe
ENST00000648256.1:c.153G>C	ENSP00000497356.1:p.Leu51Phe
ENST00000648314.1:c.204G>C	ENSP00000496920.1:p.Leu68Phe
ENST00000648599.1:c.204G>C	ENSP00000497159.1:p.Leu68Phe
ENST00000648630.1:c.198G>C	ENSP00000497887.1:p.Leu66Phe
ENST00000648682.1:c.204G>C	ENSP00000498185.1:p.Leu68Phe
ENST00000648882.1:c.*30G>C	ENSP00000497603.1:n.*30G>C
ENST00000648890.1:c.204G>C	ENSP00000497503.1:p.Leu68Phe
ENST00000648915.2:c.204G>C MANE Select	ENSP00000497160.1:p.Leu68Phe
ENST00000649688.1:c.204G>C	ENSP00000497097.1:p.Leu68Phe
ENST00000649814.1:n.253G>C
ENST00000650244.1:c.349G>C	ENSP00000497227.1:n.349G>C
ENST00000650270.1:c.71G>C
ENST00000273783.7:c.204G>C	ENSP00000273783.3:p.Leu68Phe
ENST00000432569.1:c.204G>C	ENSP00000414775.1:p.Leu68Phe
ENST00000432982.5:c.190G>C
ENST00000444495.1:c.204G>C	ENSP00000409142.1:p.Leu68Phe
ENST00000471832.1:n.135G>C
ENST00000481054.5:n.205G>C
ENST00000491144.5:n.552G>C
ENST00000498831.1:n.60G>C
NM_003907.2:c.204G>C	NP_003898.2:p.Leu68Phe
XR_924208.1:n.1155G>C
NM_003907.3:c.204G>C MANE Select	NP_003898.2:p.Leu68Phe
XM_011513266.3:c.-698G>C	XP_011511568.1:n.-698G>C
XR_001740352.2:n.567G>C
XR_001740353.2:n.567G>C
XR_924208.2:n.567G>C