Canonical Allele Identifier: CA1425882953

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137990A= , CM000665.2:g.184137990A=	GRCh38
NC_000003.11:g.183855778A= , CM000665.1:g.183855778A=	GRCh37
NC_000003.10:g.185338472A=	NCBI36
NG_015826.1:g.7969A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.622A=
ENST00000468748.7:n.582A=
ENST00000484154.2:n.1220A=
ENST00000491008.6:n.1347A=
ENST00000492226.2:n.596A=
ENST00000492773.6:c.331A=
ENST00000647636.1:c.599A=	ENSP00000497505.1:p.Asn200=
ENST00000647909.1:c.623A=	ENSP00000498164.1:p.Asn208=
ENST00000648145.1:c.367A=
ENST00000648189.1:c.349A=
ENST00000648256.1:c.548A=	ENSP00000497356.1:p.Asn183=
ENST00000648314.1:c.599A=	ENSP00000496920.1:p.Asn200=
ENST00000648599.1:c.599A=	ENSP00000497159.1:p.Asn200=
ENST00000648630.1:c.593A=	ENSP00000497887.1:p.Asn198=
ENST00000648682.1:c.599A=	ENSP00000498185.1:p.Asn200=
ENST00000648882.1:c.*425A=	ENSP00000497603.1:n.*425A=
ENST00000648890.1:c.599A=	ENSP00000497503.1:p.Asn200=
ENST00000648915.2:c.599A= MANE Select	ENSP00000497160.1:p.Asn200=
ENST00000649545.1:c.333A=
ENST00000649688.1:c.599A=	ENSP00000497097.1:p.Asn200=
ENST00000649814.1:n.648A=
ENST00000650270.1:c.466A=
ENST00000273783.7:c.599A=	ENSP00000273783.3:p.Asn200=
ENST00000432982.5:c.245+1315A=
ENST00000444495.1:c.599A=	ENSP00000409142.1:p.Asn200=
ENST00000468748.5:n.52A=
ENST00000481054.5:n.600A=
ENST00000491008.5:n.563A=
ENST00000491144.5:n.1039A=
ENST00000498831.1:n.554A=
NM_003907.2:c.599A=	NP_003898.2:p.Asn200=
XR_924208.1:n.1550A=
NM_003907.3:c.599A= MANE Select	NP_003898.2:p.Asn200=
XM_011513266.3:c.-303A=	XP_011511568.1:n.-303A=
XR_001740352.2:n.962A=
XR_001740353.2:n.962A=
XR_924208.2:n.962A=