Canonical Allele Identifier: CA355382326

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855780G>T (hg19) ; chr3:g.184137992G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137992G>T , CM000665.2:g.184137992G>T	GRCh38
NC_000003.11:g.183855780G>T , CM000665.1:g.183855780G>T	GRCh37
NC_000003.10:g.185338474G>T	NCBI36
NG_015826.1:g.7971G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.624G>T
ENST00000468748.7:n.584G>T
ENST00000484154.2:n.1222G>T
ENST00000491008.6:n.1349G>T
ENST00000492226.2:n.598G>T
ENST00000492773.6:c.333G>T
ENST00000647636.1:c.601G>T	ENSP00000497505.1:p.Val201Leu
ENST00000647909.1:c.625G>T	ENSP00000498164.1:p.Val209Leu
ENST00000648145.1:c.369G>T
ENST00000648189.1:c.351G>T
ENST00000648256.1:c.550G>T	ENSP00000497356.1:p.Val184Leu
ENST00000648314.1:c.601G>T	ENSP00000496920.1:p.Val201Leu
ENST00000648599.1:c.601G>T	ENSP00000497159.1:p.Val201Leu
ENST00000648630.1:c.595G>T	ENSP00000497887.1:p.Val199Leu
ENST00000648682.1:c.601G>T	ENSP00000498185.1:p.Val201Leu
ENST00000648882.1:c.*427G>T	ENSP00000497603.1:n.*427G>T
ENST00000648890.1:c.601G>T	ENSP00000497503.1:p.Val201Leu
ENST00000648915.2:c.601G>T MANE Select	ENSP00000497160.1:p.Val201Leu
ENST00000649545.1:c.335G>T
ENST00000649688.1:c.601G>T	ENSP00000497097.1:p.Val201Leu
ENST00000649814.1:n.650G>T
ENST00000650270.1:c.468G>T
ENST00000273783.7:c.601G>T	ENSP00000273783.3:p.Val201Leu
ENST00000432982.5:c.245+1317G>T
ENST00000444495.1:c.601G>T	ENSP00000409142.1:p.Val201Leu
ENST00000468748.5:n.54G>T
ENST00000481054.5:n.602G>T
ENST00000491008.5:n.565G>T
ENST00000491144.5:n.1041G>T
ENST00000498831.1:n.556G>T
NM_003907.2:c.601G>T	NP_003898.2:p.Val201Leu
XR_924208.1:n.1552G>T
NM_003907.3:c.601G>T MANE Select	NP_003898.2:p.Val201Leu
XM_011513266.3:c.-301G>T	XP_011511568.1:n.-301G>T
XR_001740352.2:n.964G>T
XR_001740353.2:n.964G>T
XR_924208.2:n.964G>T