Canonical Allele Identifier: CA355382392

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855813G>T (hg19) ; chr3:g.184138025G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138025G>T , CM000665.2:g.184138025G>T	GRCh38
NC_000003.11:g.183855813G>T , CM000665.1:g.183855813G>T	GRCh37
NC_000003.10:g.185338507G>T	NCBI36
NG_015826.1:g.8004G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.657G>T
ENST00000468748.7:n.617G>T
ENST00000484154.2:n.1255G>T
ENST00000491008.6:n.1382G>T
ENST00000492226.2:n.631G>T
ENST00000492773.6:c.366G>T
ENST00000647636.1:c.634G>T	ENSP00000497505.1:p.Val212Phe
ENST00000647909.1:c.658G>T	ENSP00000498164.1:p.Val220Phe
ENST00000648145.1:c.402G>T
ENST00000648189.1:c.384G>T
ENST00000648256.1:c.583G>T	ENSP00000497356.1:p.Val195Phe
ENST00000648314.1:c.634G>T	ENSP00000496920.1:p.Val212Phe
ENST00000648599.1:c.634G>T	ENSP00000497159.1:p.Val212Phe
ENST00000648630.1:c.628G>T	ENSP00000497887.1:p.Val210Phe
ENST00000648682.1:c.634G>T	ENSP00000498185.1:p.Val212Phe
ENST00000648882.1:c.*460G>T	ENSP00000497603.1:n.*460G>T
ENST00000648890.1:c.634G>T	ENSP00000497503.1:p.Val212Phe
ENST00000648915.2:c.634G>T MANE Select	ENSP00000497160.1:p.Val212Phe
ENST00000649545.1:c.368G>T
ENST00000649688.1:c.634G>T	ENSP00000497097.1:p.Val212Phe
ENST00000649814.1:n.683G>T
ENST00000650270.1:c.501G>T
ENST00000273783.7:c.634G>T	ENSP00000273783.3:p.Val212Phe
ENST00000432982.5:c.245+1350G>T
ENST00000444495.1:c.634G>T	ENSP00000409142.1:p.Val212Phe
ENST00000468748.5:n.87G>T
ENST00000481054.5:n.635G>T
ENST00000491008.5:n.598G>T
ENST00000491144.5:n.1074G>T
ENST00000498831.1:n.589G>T
NM_003907.2:c.634G>T	NP_003898.2:p.Val212Phe
XR_924208.1:n.1585G>T
NM_003907.3:c.634G>T MANE Select	NP_003898.2:p.Val212Phe
XM_011513266.3:c.-268G>T	XP_011511568.1:n.-268G>T
XR_001740352.2:n.997G>T
XR_001740353.2:n.997G>T
XR_924208.2:n.997G>T