Canonical Allele Identifier: CA2538988959

Gene: EIF2B5

Linked Data

• ClinVar Variation Id: 2725151
• ClinVar RCV Id: RCV003554471

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138154T>C , CM000665.2:g.184138154T>C	GRCh38
NC_000003.11:g.183855942T>C , CM000665.1:g.183855942T>C	GRCh37
NC_000003.10:g.185338636T>C	NCBI36
NG_015826.1:g.8133T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.708-12T>C
ENST00000468748.7:n.668-12T>C
ENST00000484154.2:n.1306-12T>C
ENST00000491008.6:n.1433-12T>C
ENST00000492226.2:n.682-12T>C
ENST00000492773.6:c.427T>C
ENST00000647636.1:c.685-12T>C	ENSP00000497505.1:n.685-12T>C
ENST00000647909.1:c.709-12T>C	ENSP00000498164.1:n.709-12T>C
ENST00000648145.1:c.453-12T>C
ENST00000648189.1:c.435-12T>C
ENST00000648256.1:c.634-12T>C	ENSP00000497356.1:n.634-12T>C
ENST00000648314.1:c.685-12T>C	ENSP00000496920.1:n.685-12T>C
ENST00000648599.1:c.685-12T>C	ENSP00000497159.1:n.685-12T>C
ENST00000648630.1:c.679-12T>C	ENSP00000497887.1:n.679-12T>C
ENST00000648682.1:c.685-12T>C	ENSP00000498185.1:n.685-12T>C
ENST00000648882.1:c.*511-12T>C	ENSP00000497603.1:n.*511-12T>C
ENST00000648890.1:c.685-12T>C	ENSP00000497503.1:n.685-12T>C
ENST00000648915.2:c.685-12T>C MANE Select	ENSP00000497160.1:n.685-12T>C
ENST00000649545.1:c.419-12T>C
ENST00000649688.1:c.685-12T>C	ENSP00000497097.1:n.685-12T>C
ENST00000649814.1:n.734-12T>C
ENST00000650270.1:c.552-12T>C
ENST00000273783.7:c.685-12T>C	ENSP00000273783.3:n.685-12T>C
ENST00000432982.5:c.245+1479T>C
ENST00000444495.1:c.685-12T>C	ENSP00000409142.1:n.685-12T>C
ENST00000468748.5:n.138-12T>C
ENST00000481054.5:n.686-12T>C
ENST00000491008.5:n.649-12T>C
ENST00000491144.5:n.1125-12T>C
NM_003907.2:c.685-12T>C	NP_003898.2:n.685-12T>C
XR_924208.1:n.1636-12T>C
NM_003907.3:c.685-12T>C MANE Select	NP_003898.2:n.685-12T>C
XM_011513266.3:c.-217-12T>C	XP_011511568.1:n.-217-12T>C
XR_001740352.2:n.1048-12T>C
XR_001740353.2:n.1048-12T>C
XR_924208.2:n.1048-12T>C