Canonical Allele Identifier: CA2580068295

Gene: EIF2AK3

Linked Data

• ClinVar Variation Id: 2126497
• ClinVar RCV Id: RCV003051691

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88583428dup , CM000664.2:g.88583428dup	GRCh38
NC_000002.11:g.88882946dup , CM000664.1:g.88882946dup	GRCh37
NC_000002.10:g.88664061dup	NCBI36
NG_016424.1:g.49149dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682276.1:n.1208+2dup
ENST00000682892.1:c.1310+2dup	ENSP00000507214.1:n.1310+2dup
ENST00000682952.1:n.1402+2dup
ENST00000684455.1:c.976+2dup
ENST00000684642.1:c.1160+2dup	ENSP00000507355.1:n.1160+2dup
ENST00000303236.9:c.1763+2dup MANE Select	ENSP00000307235.3:n.1763+2dup
ENST00000652099.1:c.1957+2dup
ENST00000652736.1:n.1639+2dup
ENST00000303236.7:c.1763+2dup	ENSP00000307235.3:n.1763+2dup
ENST00000415570.1:c.1400+2dup	ENSP00000412076.1:n.1400+2dup
ENST00000419748.5:c.1310+2dup	ENSP00000408325.1:n.1310+2dup
NM_001313915.1:c.1310+2dup	NP_001300844.1:n.1310+2dup
NM_004836.5:c.1763+2dup	NP_004827.4:n.1763+2dup
NM_004836.6:c.1763+2dup	NP_004827.4:n.1763+2dup
XM_005264649.3:c.1079+2dup	XP_005264706.1:n.1079+2dup
XR_939749.1:n.1972+2dup
XM_017005376.2:c.1079+2dup	XP_016860865.1:n.1079+2dup
NM_004836.7:c.1763+2dup MANE Select	NP_004827.4:n.1763+2dup
NM_001313915.2:c.1310+2dup	NP_001300844.1:n.1310+2dup