Canonical Allele Identifier: CA355382963

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855988T>C (hg19) ; chr3:g.184138200T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138200T>C , CM000665.2:g.184138200T>C	GRCh38
NC_000003.11:g.183855988T>C , CM000665.1:g.183855988T>C	GRCh37
NC_000003.10:g.185338682T>C	NCBI36
NG_015826.1:g.8179T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.742T>C
ENST00000468748.7:n.702T>C
ENST00000484154.2:n.1340T>C
ENST00000491008.6:n.1467T>C
ENST00000492226.2:n.716T>C
ENST00000492773.6:c.473T>C
ENST00000647636.1:c.719T>C	ENSP00000497505.1:p.Val240Ala
ENST00000647909.1:c.743T>C	ENSP00000498164.1:p.Val248Ala
ENST00000648145.1:c.487T>C
ENST00000648189.1:c.469T>C
ENST00000648256.1:c.668T>C	ENSP00000497356.1:p.Val223Ala
ENST00000648314.1:c.719T>C	ENSP00000496920.1:p.Val240Ala
ENST00000648599.1:c.719T>C	ENSP00000497159.1:p.Val240Ala
ENST00000648630.1:c.713T>C	ENSP00000497887.1:p.Val238Ala
ENST00000648682.1:c.719T>C	ENSP00000498185.1:p.Val240Ala
ENST00000648882.1:c.*545T>C	ENSP00000497603.1:n.*545T>C
ENST00000648890.1:c.719T>C	ENSP00000497503.1:p.Val240Ala
ENST00000648915.2:c.719T>C MANE Select	ENSP00000497160.1:p.Val240Ala
ENST00000649545.1:c.453T>C
ENST00000649688.1:c.719T>C	ENSP00000497097.1:p.Val240Ala
ENST00000649814.1:n.768T>C
ENST00000650270.1:c.586T>C
ENST00000273783.7:c.719T>C	ENSP00000273783.3:p.Val240Ala
ENST00000432982.5:c.245+1525T>C
ENST00000444495.1:c.719T>C	ENSP00000409142.1:p.Val240Ala
ENST00000468748.5:n.172T>C
ENST00000479833.1:n.35T>C
ENST00000481054.5:n.720T>C
ENST00000491008.5:n.683T>C
ENST00000491144.5:n.1159T>C
NM_003907.2:c.719T>C	NP_003898.2:p.Val240Ala
XR_924208.1:n.1670T>C
NM_003907.3:c.719T>C MANE Select	NP_003898.2:p.Val240Ala
XM_011513266.3:c.-183T>C	XP_011511568.1:n.-183T>C
XR_001740352.2:n.1082T>C
XR_001740353.2:n.1082T>C
XR_924208.2:n.1082T>C