Canonical Allele Identifier: CA2668795854

Gene: EIF2B5

Linked Data

• gnomAD v4: 3-184135379-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184135379G>A , CM000665.2:g.184135379G>A	GRCh38
NC_000003.11:g.183853167G>A , CM000665.1:g.183853167G>A	GRCh37
NC_000003.10:g.185335861G>A	NCBI36
NG_015826.1:g.5358G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432569.2:c.-7G>A	ENSP00000414775.1:n.-7G>A
ENST00000465218.3:n.17G>A
ENST00000471832.2:c.-7G>A	ENSP00000497786.1:n.-7G>A
ENST00000647636.1:c.-7G>A	ENSP00000497505.1:n.-7G>A
ENST00000647909.1:c.-7G>A	ENSP00000498164.1:n.-7G>A
ENST00000648314.1:c.-7G>A	ENSP00000496920.1:n.-7G>A
ENST00000648599.1:c.-7G>A	ENSP00000497159.1:n.-7G>A
ENST00000648682.1:c.-7G>A	ENSP00000498185.1:n.-7G>A
ENST00000648890.1:c.-7G>A	ENSP00000497503.1:n.-7G>A
ENST00000648915.2:c.-7G>A MANE Select	ENSP00000497160.1:n.-7G>A
ENST00000649688.1:c.-7G>A	ENSP00000497097.1:n.-7G>A
ENST00000649814.1:n.43G>A
ENST00000273783.7:c.-7G>A	ENSP00000273783.3:n.-7G>A
ENST00000432569.1:c.-7G>A	ENSP00000414775.1:n.-7G>A
ENST00000444495.1:c.-7G>A	ENSP00000409142.1:n.-7G>A
ENST00000491144.5:n.342G>A
NM_003907.2:c.-7G>A	NP_003898.2:n.-7G>A
XR_924208.1:n.945G>A
NM_003907.3:c.-7G>A MANE Select	NP_003898.2:n.-7G>A
XM_011513266.3:c.-908G>A	XP_011511568.1:n.-908G>A
XR_001740352.2:n.357G>A
XR_001740353.2:n.357G>A
XR_924208.2:n.357G>A