Canonical Allele Identifier: CA355382282

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855760C>A (hg19) ; chr3:g.184137972C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137972C>A , CM000665.2:g.184137972C>A	GRCh38
NC_000003.11:g.183855760C>A , CM000665.1:g.183855760C>A	GRCh37
NC_000003.10:g.185338454C>A	NCBI36
NG_015826.1:g.7951C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.604C>A
ENST00000468748.7:n.564C>A
ENST00000484154.2:n.1202C>A
ENST00000491008.6:n.1329C>A
ENST00000492226.2:n.578C>A
ENST00000492773.6:c.313C>A
ENST00000647636.1:c.581C>A	ENSP00000497505.1:p.Thr194Asn
ENST00000647909.1:c.605C>A	ENSP00000498164.1:p.Thr202Asn
ENST00000648145.1:c.349C>A
ENST00000648189.1:c.331C>A
ENST00000648256.1:c.530C>A	ENSP00000497356.1:p.Thr177Asn
ENST00000648314.1:c.581C>A	ENSP00000496920.1:p.Thr194Asn
ENST00000648599.1:c.581C>A	ENSP00000497159.1:p.Thr194Asn
ENST00000648630.1:c.575C>A	ENSP00000497887.1:p.Thr192Asn
ENST00000648682.1:c.581C>A	ENSP00000498185.1:p.Thr194Asn
ENST00000648882.1:c.*407C>A	ENSP00000497603.1:n.*407C>A
ENST00000648890.1:c.581C>A	ENSP00000497503.1:p.Thr194Asn
ENST00000648915.2:c.581C>A MANE Select	ENSP00000497160.1:p.Thr194Asn
ENST00000649545.1:c.315C>A
ENST00000649688.1:c.581C>A	ENSP00000497097.1:p.Thr194Asn
ENST00000649814.1:n.630C>A
ENST00000650270.1:c.448C>A
ENST00000273783.7:c.581C>A	ENSP00000273783.3:p.Thr194Asn
ENST00000432982.5:c.245+1297C>A
ENST00000444495.1:c.581C>A	ENSP00000409142.1:p.Thr194Asn
ENST00000468748.5:n.34C>A
ENST00000481054.5:n.582C>A
ENST00000491008.5:n.545C>A
ENST00000491144.5:n.1021C>A
ENST00000498831.1:n.536C>A
NM_003907.2:c.581C>A	NP_003898.2:p.Thr194Asn
XR_924208.1:n.1532C>A
NM_003907.3:c.581C>A MANE Select	NP_003898.2:p.Thr194Asn
XM_011513266.3:c.-321C>A	XP_011511568.1:n.-321C>A
XR_001740352.2:n.944C>A
XR_001740353.2:n.944C>A
XR_924208.2:n.944C>A