Canonical Allele Identifier: CA894275456

Gene: EIF2AK3

Linked Data

• dbSNP Id: rs1360882682
• gnomAD v3: 2-88575594-CA-C
• gnomAD v4: 2-88575594-CA-C
• MyVariant Identifiers: chr2:g.88875113del (hg19) ; chr2:g.88575595del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575596del , CM000664.2:g.88575596del	GRCh38
NC_000002.11:g.88875114del , CM000664.1:g.88875114del	GRCh37
NC_000002.10:g.88656229del	NCBI36
NG_016424.1:g.56982del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1865-149del
ENST00000682276.1:n.1482-149del
ENST00000682892.1:c.1584-149del	ENSP00000507214.1:n.1584-149del
ENST00000682952.1:n.1676-149del
ENST00000684455.1:c.1250-149del
ENST00000684642.1:c.1434-149del	ENSP00000507355.1:n.1434-149del
ENST00000684740.1:n.2215-149del
ENST00000303236.9:c.2037-149del MANE Select	ENSP00000307235.3:n.2037-149del
ENST00000652099.1:c.2231-149del
ENST00000652736.1:n.1913-149del
ENST00000303236.7:c.2037-149del	ENSP00000307235.3:n.2037-149del
ENST00000415570.1:c.1674-149del	ENSP00000412076.1:n.1674-149del
ENST00000419748.5:c.1584-149del	ENSP00000408325.1:n.1584-149del
ENST00000478003.1:n.603-149del
NM_001313915.1:c.1584-149del	NP_001300844.1:n.1584-149del
NM_004836.5:c.2037-149del	NP_004827.4:n.2037-149del
NM_004836.6:c.2037-149del	NP_004827.4:n.2037-149del
NR_110236.1:n.1733del
XM_005264649.3:c.1353-149del	XP_005264706.1:n.1353-149del
XR_939749.1:n.2316-149del
XM_017005376.2:c.1353-149del	XP_016860865.1:n.1353-149del
NM_004836.7:c.2037-149del MANE Select	NP_004827.4:n.2037-149del
NM_001313915.2:c.1584-149del	NP_001300844.1:n.1584-149del