Canonical Allele Identifier: CA1425887000

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184141803G= , CM000665.2:g.184141803G=	GRCh38
NC_000003.11:g.183859591G= , CM000665.1:g.183859591G=	GRCh37
NC_000003.10:g.185342285G=	NCBI36
NG_015826.1:g.11782G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.1180-122G=
ENST00000468748.7:n.1400-122G=
ENST00000484154.2:n.1387-122G=
ENST00000491008.6:n.1905-122G=
ENST00000492226.2:n.1424-122G=
ENST00000492773.6:c.911-122G=
ENST00000647636.1:c.1157-64G=	ENSP00000497505.1:n.1157-64G=
ENST00000647909.1:c.1181-122G=	ENSP00000498164.1:n.1181-122G=
ENST00000648145.1:c.925-118G=
ENST00000648189.1:c.971-118G=
ENST00000648256.1:c.1129-122G=	ENSP00000497356.1:n.1129-122G=
ENST00000648314.1:c.*276-122G=	ENSP00000496920.1:n.*276-122G=
ENST00000648599.1:c.*440-122G=	ENSP00000497159.1:n.*440-122G=
ENST00000648630.1:c.1036-122G=	ENSP00000497887.1:n.1036-122G=
ENST00000648682.1:c.1167-122G=	ENSP00000498185.1:n.1167-122G=
ENST00000648882.1:c.*983-122G=	ENSP00000497603.1:n.*983-122G=
ENST00000648890.1:c.1157-122G=	ENSP00000497503.1:n.1157-122G=
ENST00000648915.2:c.1157-122G= MANE Select	ENSP00000497160.1:n.1157-122G=
ENST00000649545.1:c.578-122G=
ENST00000649688.1:c.*450-122G=	ENSP00000497097.1:n.*450-122G=
ENST00000649814.1:n.1206-122G=
ENST00000650270.1:c.1024-122G=
ENST00000273783.7:c.1157-122G=	ENSP00000273783.3:n.1157-122G=
ENST00000432982.5:c.246-434G=
ENST00000444495.1:c.1157-122G=	ENSP00000409142.1:n.1157-122G=
ENST00000479833.1:n.358-122G=
ENST00000481054.5:n.1251-122G=
ENST00000491144.5:n.1661-122G=
ENST00000492773.5:n.40-122G=
NM_003907.2:c.1157-122G=	NP_003898.2:n.1157-122G=
XM_011513265.1:c.407-122G=	XP_011511567.1:n.407-122G=
XM_011513266.1:c.320-122G=	XP_011511568.1:n.320-122G=
XR_924208.1:n.2108-122G=
NM_003907.3:c.1157-122G= MANE Select	NP_003898.2:n.1157-122G=
XM_011513266.3:c.320-122G=	XP_011511568.1:n.320-122G=
XR_001740352.2:n.1520-122G=
XR_001740353.2:n.1520-122G=
XR_924208.2:n.1520-122G=