Canonical Allele Identifier: CA437146677

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183856007T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138219T>C , CM000665.2:g.184138219T>C	GRCh38
NC_000003.11:g.183856007T>C , CM000665.1:g.183856007T>C	GRCh37
NC_000003.10:g.185338701T>C	NCBI36
NG_015826.1:g.8198T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.761T>C
ENST00000468748.7:n.721T>C
ENST00000484154.2:n.1359T>C
ENST00000491008.6:n.1486T>C
ENST00000492226.2:n.735T>C
ENST00000492773.6:c.492T>C
ENST00000647636.1:c.738T>C	ENSP00000497505.1:p.Asp246=
ENST00000647909.1:c.762T>C	ENSP00000498164.1:p.Asp254=
ENST00000648145.1:c.506T>C
ENST00000648189.1:c.488T>C
ENST00000648256.1:c.687T>C	ENSP00000497356.1:p.Asp229=
ENST00000648314.1:c.738T>C	ENSP00000496920.1:p.Asp246=
ENST00000648599.1:c.738T>C	ENSP00000497159.1:p.Asp246=
ENST00000648630.1:c.732T>C	ENSP00000497887.1:p.Asp244=
ENST00000648682.1:c.738T>C	ENSP00000498185.1:p.Asp246=
ENST00000648882.1:c.*564T>C	ENSP00000497603.1:n.*564T>C
ENST00000648890.1:c.738T>C	ENSP00000497503.1:p.Asp246=
ENST00000648915.2:c.738T>C MANE Select	ENSP00000497160.1:p.Asp246=
ENST00000649545.1:c.472T>C
ENST00000649688.1:c.738T>C	ENSP00000497097.1:p.Asp246=
ENST00000649814.1:n.787T>C
ENST00000650270.1:c.605T>C
ENST00000273783.7:c.738T>C	ENSP00000273783.3:p.Asp246=
ENST00000432982.5:c.245+1544T>C
ENST00000444495.1:c.738T>C	ENSP00000409142.1:p.Asp246=
ENST00000468748.5:n.191T>C
ENST00000479833.1:n.54T>C
ENST00000481054.5:n.739T>C
ENST00000491008.5:n.702T>C
ENST00000491144.5:n.1178T>C
NM_003907.2:c.738T>C	NP_003898.2:p.Asp246=
XR_924208.1:n.1689T>C
NM_003907.3:c.738T>C MANE Select	NP_003898.2:p.Asp246=
XM_011513266.3:c.-164T>C	XP_011511568.1:n.-164T>C
XR_001740352.2:n.1101T>C
XR_001740353.2:n.1101T>C
XR_924208.2:n.1101T>C