Canonical Allele Identifier: CA355382882

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855970G>C (hg19) ; chr3:g.184138182G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138182G>C , CM000665.2:g.184138182G>C	GRCh38
NC_000003.11:g.183855970G>C , CM000665.1:g.183855970G>C	GRCh37
NC_000003.10:g.185338664G>C	NCBI36
NG_015826.1:g.8161G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.724G>C
ENST00000468748.7:n.684G>C
ENST00000484154.2:n.1322G>C
ENST00000491008.6:n.1449G>C
ENST00000492226.2:n.698G>C
ENST00000492773.6:c.455G>C
ENST00000647636.1:c.701G>C	ENSP00000497505.1:p.Ser234Thr
ENST00000647909.1:c.725G>C	ENSP00000498164.1:p.Ser242Thr
ENST00000648145.1:c.469G>C
ENST00000648189.1:c.451G>C
ENST00000648256.1:c.650G>C	ENSP00000497356.1:p.Ser217Thr
ENST00000648314.1:c.701G>C	ENSP00000496920.1:p.Ser234Thr
ENST00000648599.1:c.701G>C	ENSP00000497159.1:p.Ser234Thr
ENST00000648630.1:c.695G>C	ENSP00000497887.1:p.Ser232Thr
ENST00000648682.1:c.701G>C	ENSP00000498185.1:p.Ser234Thr
ENST00000648882.1:c.*527G>C	ENSP00000497603.1:n.*527G>C
ENST00000648890.1:c.701G>C	ENSP00000497503.1:p.Ser234Thr
ENST00000648915.2:c.701G>C MANE Select	ENSP00000497160.1:p.Ser234Thr
ENST00000649545.1:c.435G>C
ENST00000649688.1:c.701G>C	ENSP00000497097.1:p.Ser234Thr
ENST00000649814.1:n.750G>C
ENST00000650270.1:c.568G>C
ENST00000273783.7:c.701G>C	ENSP00000273783.3:p.Ser234Thr
ENST00000432982.5:c.245+1507G>C
ENST00000444495.1:c.701G>C	ENSP00000409142.1:p.Ser234Thr
ENST00000468748.5:n.154G>C
ENST00000479833.1:n.17G>C
ENST00000481054.5:n.702G>C
ENST00000491008.5:n.665G>C
ENST00000491144.5:n.1141G>C
NM_003907.2:c.701G>C	NP_003898.2:p.Ser234Thr
XR_924208.1:n.1652G>C
NM_003907.3:c.701G>C MANE Select	NP_003898.2:p.Ser234Thr
XM_011513266.3:c.-201G>C	XP_011511568.1:n.-201G>C
XR_001740352.2:n.1064G>C
XR_001740353.2:n.1064G>C
XR_924208.2:n.1064G>C