Canonical Allele Identifier: CA355381856

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855476C>G (hg19) ; chr3:g.184137688C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137688C>G , CM000665.2:g.184137688C>G	GRCh38
NC_000003.11:g.183855476C>G , CM000665.1:g.183855476C>G	GRCh37
NC_000003.10:g.185338170C>G	NCBI36
NG_015826.1:g.7667C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000465218.3:n.412C>G
ENST00000468748.7:n.372C>G
ENST00000484154.2:n.1010C>G
ENST00000491008.6:n.1137C>G
ENST00000492226.2:n.386C>G
ENST00000492773.6:c.121C>G
ENST00000647636.1:c.389C>G	ENSP00000497505.1:p.Ser130Ter
ENST00000647909.1:c.389C>G	ENSP00000498164.1:p.Ser130Ter
ENST00000648145.1:c.157C>G
ENST00000648189.1:c.139C>G
ENST00000648256.1:c.338C>G	ENSP00000497356.1:p.Ser113Ter
ENST00000648314.1:c.389C>G	ENSP00000496920.1:p.Ser130Ter
ENST00000648599.1:c.389C>G	ENSP00000497159.1:p.Ser130Ter
ENST00000648630.1:c.383C>G	ENSP00000497887.1:p.Ser128Ter
ENST00000648682.1:c.389C>G	ENSP00000498185.1:p.Ser130Ter
ENST00000648882.1:c.*215C>G	ENSP00000497603.1:n.*215C>G
ENST00000648890.1:c.389C>G	ENSP00000497503.1:p.Ser130Ter
ENST00000648915.2:c.389C>G MANE Select	ENSP00000497160.1:p.Ser130Ter
ENST00000649545.1:c.123C>G
ENST00000649688.1:c.389C>G	ENSP00000497097.1:p.Ser130Ter
ENST00000649814.1:n.438C>G
ENST00000650244.1:c.534C>G	ENSP00000497227.1:n.534C>G
ENST00000650270.1:c.256C>G
ENST00000273783.7:c.389C>G	ENSP00000273783.3:p.Ser130Ter
ENST00000432982.5:c.245+1013C>G
ENST00000444495.1:c.389C>G	ENSP00000409142.1:p.Ser130Ter
ENST00000481054.5:n.390C>G
ENST00000491008.5:n.353C>G
ENST00000491144.5:n.737C>G
ENST00000498831.1:n.344C>G
NM_003907.2:c.389C>G	NP_003898.2:p.Ser130Ter
XR_924208.1:n.1340C>G
NM_003907.3:c.389C>G MANE Select	NP_003898.2:p.Ser130Ter
XM_011513266.3:c.-513C>G	XP_011511568.1:n.-513C>G
XR_001740352.2:n.752C>G
XR_001740353.2:n.752C>G
XR_924208.2:n.752C>G