Canonical Allele Identifier: CA51491884

Gene: EIF2AK3

Linked Data

• dbSNP Id: rs925488478
• gnomAD v3: 2-88583356-TA-T
• gnomAD v4: 2-88583356-TA-T
• MyVariant Identifiers: chr2:g.88882875del (hg19) ; chr2:g.88583357del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88583365del , CM000664.2:g.88583365del	GRCh38
NC_000002.11:g.88882883del , CM000664.1:g.88882883del	GRCh37
NC_000002.10:g.88663998del	NCBI36
NG_016424.1:g.49220del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682276.1:n.1208+73del
ENST00000682892.1:c.1310+73del	ENSP00000507214.1:n.1310+73del
ENST00000682952.1:n.1402+73del
ENST00000684455.1:c.976+73del
ENST00000684642.1:c.1160+73del	ENSP00000507355.1:n.1160+73del
ENST00000303236.9:c.1763+73del MANE Select	ENSP00000307235.3:n.1763+73del
ENST00000652099.1:c.1957+73del
ENST00000652736.1:n.1639+73del
ENST00000303236.7:c.1763+73del	ENSP00000307235.3:n.1763+73del
ENST00000415570.1:c.1400+73del	ENSP00000412076.1:n.1400+73del
ENST00000419748.5:c.1310+73del	ENSP00000408325.1:n.1310+73del
NM_001313915.1:c.1310+73del	NP_001300844.1:n.1310+73del
NM_004836.5:c.1763+73del	NP_004827.4:n.1763+73del
NM_004836.6:c.1763+73del	NP_004827.4:n.1763+73del
XM_005264649.3:c.1079+73del	XP_005264706.1:n.1079+73del
XR_939749.1:n.1972+73del
XM_017005376.2:c.1079+73del	XP_016860865.1:n.1079+73del
NM_004836.7:c.1763+73del MANE Select	NP_004827.4:n.1763+73del
NM_001313915.2:c.1310+73del	NP_001300844.1:n.1310+73del