Canonical Allele Identifier: CA355382319

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855777A>G (hg19) ; chr3:g.184137989A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137989A>G , CM000665.2:g.184137989A>G	GRCh38
NC_000003.11:g.183855777A>G , CM000665.1:g.183855777A>G	GRCh37
NC_000003.10:g.185338471A>G	NCBI36
NG_015826.1:g.7968A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.621A>G
ENST00000468748.7:n.581A>G
ENST00000484154.2:n.1219A>G
ENST00000491008.6:n.1346A>G
ENST00000492226.2:n.595A>G
ENST00000492773.6:c.330A>G
ENST00000647636.1:c.598A>G	ENSP00000497505.1:p.Asn200Asp
ENST00000647909.1:c.622A>G	ENSP00000498164.1:p.Asn208Asp
ENST00000648145.1:c.366A>G
ENST00000648189.1:c.348A>G
ENST00000648256.1:c.547A>G	ENSP00000497356.1:p.Asn183Asp
ENST00000648314.1:c.598A>G	ENSP00000496920.1:p.Asn200Asp
ENST00000648599.1:c.598A>G	ENSP00000497159.1:p.Asn200Asp
ENST00000648630.1:c.592A>G	ENSP00000497887.1:p.Asn198Asp
ENST00000648682.1:c.598A>G	ENSP00000498185.1:p.Asn200Asp
ENST00000648882.1:c.*424A>G	ENSP00000497603.1:n.*424A>G
ENST00000648890.1:c.598A>G	ENSP00000497503.1:p.Asn200Asp
ENST00000648915.2:c.598A>G MANE Select	ENSP00000497160.1:p.Asn200Asp
ENST00000649545.1:c.332A>G
ENST00000649688.1:c.598A>G	ENSP00000497097.1:p.Asn200Asp
ENST00000649814.1:n.647A>G
ENST00000650270.1:c.465A>G
ENST00000273783.7:c.598A>G	ENSP00000273783.3:p.Asn200Asp
ENST00000432982.5:c.245+1314A>G
ENST00000444495.1:c.598A>G	ENSP00000409142.1:p.Asn200Asp
ENST00000468748.5:n.51A>G
ENST00000481054.5:n.599A>G
ENST00000491008.5:n.562A>G
ENST00000491144.5:n.1038A>G
ENST00000498831.1:n.553A>G
NM_003907.2:c.598A>G	NP_003898.2:p.Asn200Asp
XR_924208.1:n.1549A>G
NM_003907.3:c.598A>G MANE Select	NP_003898.2:p.Asn200Asp
XM_011513266.3:c.-304A>G	XP_011511568.1:n.-304A>G
XR_001740352.2:n.961A>G
XR_001740353.2:n.961A>G
XR_924208.2:n.961A>G