Canonical Allele Identifier: CA355382313

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855775A>C (hg19) ; chr3:g.184137987A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137987A>C , CM000665.2:g.184137987A>C	GRCh38
NC_000003.11:g.183855775A>C , CM000665.1:g.183855775A>C	GRCh37
NC_000003.10:g.185338469A>C	NCBI36
NG_015826.1:g.7966A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.619A>C
ENST00000468748.7:n.579A>C
ENST00000484154.2:n.1217A>C
ENST00000491008.6:n.1344A>C
ENST00000492226.2:n.593A>C
ENST00000492773.6:c.328A>C
ENST00000647636.1:c.596A>C	ENSP00000497505.1:p.Asp199Ala
ENST00000647909.1:c.620A>C	ENSP00000498164.1:p.Asp207Ala
ENST00000648145.1:c.364A>C
ENST00000648189.1:c.346A>C
ENST00000648256.1:c.545A>C	ENSP00000497356.1:p.Asp182Ala
ENST00000648314.1:c.596A>C	ENSP00000496920.1:p.Asp199Ala
ENST00000648599.1:c.596A>C	ENSP00000497159.1:p.Asp199Ala
ENST00000648630.1:c.590A>C	ENSP00000497887.1:p.Asp197Ala
ENST00000648682.1:c.596A>C	ENSP00000498185.1:p.Asp199Ala
ENST00000648882.1:c.*422A>C	ENSP00000497603.1:n.*422A>C
ENST00000648890.1:c.596A>C	ENSP00000497503.1:p.Asp199Ala
ENST00000648915.2:c.596A>C MANE Select	ENSP00000497160.1:p.Asp199Ala
ENST00000649545.1:c.330A>C
ENST00000649688.1:c.596A>C	ENSP00000497097.1:p.Asp199Ala
ENST00000649814.1:n.645A>C
ENST00000650270.1:c.463A>C
ENST00000273783.7:c.596A>C	ENSP00000273783.3:p.Asp199Ala
ENST00000432982.5:c.245+1312A>C
ENST00000444495.1:c.596A>C	ENSP00000409142.1:p.Asp199Ala
ENST00000468748.5:n.49A>C
ENST00000481054.5:n.597A>C
ENST00000491008.5:n.560A>C
ENST00000491144.5:n.1036A>C
ENST00000498831.1:n.551A>C
NM_003907.2:c.596A>C	NP_003898.2:p.Asp199Ala
XR_924208.1:n.1547A>C
NM_003907.3:c.596A>C MANE Select	NP_003898.2:p.Asp199Ala
XM_011513266.3:c.-306A>C	XP_011511568.1:n.-306A>C
XR_001740352.2:n.959A>C
XR_001740353.2:n.959A>C
XR_924208.2:n.959A>C