Canonical Allele Identifier: CA355382118

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855686G>C (hg19) ; chr3:g.184137898G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137898G>C , CM000665.2:g.184137898G>C	GRCh38
NC_000003.11:g.183855686G>C , CM000665.1:g.183855686G>C	GRCh37
NC_000003.10:g.185338380G>C	NCBI36
NG_015826.1:g.7877G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.530G>C
ENST00000468748.7:n.490G>C
ENST00000484154.2:n.1128G>C
ENST00000491008.6:n.1255G>C
ENST00000492226.2:n.504G>C
ENST00000492773.6:c.239G>C
ENST00000647636.1:c.507G>C	ENSP00000497505.1:p.Arg169Ser
ENST00000647909.1:c.531G>C	ENSP00000498164.1:p.Arg177Ser
ENST00000648145.1:c.275G>C
ENST00000648189.1:c.257G>C
ENST00000648256.1:c.456G>C	ENSP00000497356.1:p.Arg152Ser
ENST00000648314.1:c.507G>C	ENSP00000496920.1:p.Arg169Ser
ENST00000648599.1:c.507G>C	ENSP00000497159.1:p.Arg169Ser
ENST00000648630.1:c.501G>C	ENSP00000497887.1:p.Arg167Ser
ENST00000648682.1:c.507G>C	ENSP00000498185.1:p.Arg169Ser
ENST00000648882.1:c.*333G>C	ENSP00000497603.1:n.*333G>C
ENST00000648890.1:c.507G>C	ENSP00000497503.1:p.Arg169Ser
ENST00000648915.2:c.507G>C MANE Select	ENSP00000497160.1:p.Arg169Ser
ENST00000649545.1:c.241G>C
ENST00000649688.1:c.507G>C	ENSP00000497097.1:p.Arg169Ser
ENST00000649814.1:n.556G>C
ENST00000650244.1:c.652G>C	ENSP00000497227.1:n.652G>C
ENST00000650270.1:c.374G>C
ENST00000273783.7:c.507G>C	ENSP00000273783.3:p.Arg169Ser
ENST00000432982.5:c.245+1223G>C
ENST00000444495.1:c.507G>C	ENSP00000409142.1:p.Arg169Ser
ENST00000481054.5:n.508G>C
ENST00000491008.5:n.471G>C
ENST00000491144.5:n.947G>C
ENST00000498831.1:n.462G>C
NM_003907.2:c.507G>C	NP_003898.2:p.Arg169Ser
XR_924208.1:n.1458G>C
NM_003907.3:c.507G>C MANE Select	NP_003898.2:p.Arg169Ser
XM_011513266.3:c.-395G>C	XP_011511568.1:n.-395G>C
XR_001740352.2:n.870G>C
XR_001740353.2:n.870G>C
XR_924208.2:n.870G>C