Canonical Allele Identifier: CA437323645

Gene: EIF2B5

Linked Data

• gnomAD v4: 3-184138073-C-T
• MyVariant Identifiers: chr3:g.183855861C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138073C>T , CM000665.2:g.184138073C>T	GRCh38
NC_000003.11:g.183855861C>T , CM000665.1:g.183855861C>T	GRCh37
NC_000003.10:g.185338555C>T	NCBI36
NG_015826.1:g.8052C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.705C>T
ENST00000468748.7:n.665C>T
ENST00000484154.2:n.1303C>T
ENST00000491008.6:n.1430C>T
ENST00000492226.2:n.679C>T
ENST00000492773.6:c.414C>T
ENST00000647636.1:c.682C>T	ENSP00000497505.1:p.Leu228=
ENST00000647909.1:c.706C>T	ENSP00000498164.1:p.Leu236=
ENST00000648145.1:c.450C>T
ENST00000648189.1:c.432C>T
ENST00000648256.1:c.631C>T	ENSP00000497356.1:p.Leu211=
ENST00000648314.1:c.682C>T	ENSP00000496920.1:p.Leu228=
ENST00000648599.1:c.682C>T	ENSP00000497159.1:p.Leu228=
ENST00000648630.1:c.676C>T	ENSP00000497887.1:p.Leu226=
ENST00000648682.1:c.682C>T	ENSP00000498185.1:p.Leu228=
ENST00000648882.1:c.*508C>T	ENSP00000497603.1:n.*508C>T
ENST00000648890.1:c.682C>T	ENSP00000497503.1:p.Leu228=
ENST00000648915.2:c.682C>T MANE Select	ENSP00000497160.1:p.Leu228=
ENST00000649545.1:c.416C>T
ENST00000649688.1:c.682C>T	ENSP00000497097.1:p.Leu228=
ENST00000649814.1:n.731C>T
ENST00000650270.1:c.549C>T
ENST00000273783.7:c.682C>T	ENSP00000273783.3:p.Leu228=
ENST00000432982.5:c.245+1398C>T
ENST00000444495.1:c.682C>T	ENSP00000409142.1:p.Leu228=
ENST00000468748.5:n.135C>T
ENST00000481054.5:n.683C>T
ENST00000491008.5:n.646C>T
ENST00000491144.5:n.1122C>T
NM_003907.2:c.682C>T	NP_003898.2:p.Leu228=
XR_924208.1:n.1633C>T
NM_003907.3:c.682C>T MANE Select	NP_003898.2:p.Leu228=
XM_011513266.3:c.-220C>T	XP_011511568.1:n.-220C>T
XR_001740352.2:n.1045C>T
XR_001740353.2:n.1045C>T
XR_924208.2:n.1045C>T