Canonical Allele Identifier: CA346199403

Gene: EIF2B4

Linked Data

• MyVariant Identifiers: chr2:g.27590422G>C (hg19) ; chr2:g.27367555G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27367555G>C , CM000664.2:g.27367555G>C	GRCh38
NC_000002.11:g.27590422G>C , CM000664.1:g.27590422G>C	GRCh37
NC_000002.10:g.27443926G>C	NCBI36
NG_009305.1:g.7903C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.787C>G MANE Select	ENSP00000233552.6:p.Leu263Val
ENST00000347454.8:c.787C>G	ENSP00000233552.5:p.Leu263Val
ENST00000405940.6:c.*53C>G	ENSP00000384375.2:n.*53C>G
ENST00000417567.1:c.363C>G
ENST00000445933.6:c.784C>G	ENSP00000394397.2:p.Leu262Val
ENST00000451130.6:c.847C>G	ENSP00000394869.2:p.Leu283Val
ENST00000475582.5:n.2296C>G
ENST00000493344.6:c.850C>G	ENSP00000429323.1:p.Leu284Val
ENST00000616081.4:c.778C>G	ENSP00000477710.1:p.Leu260Val
ENST00000622434.4:c.*53C>G	ENSP00000479991.1:n.*53C>G
NM_001034116.1:c.787C>G	NP_001029288.1:p.Leu263Val
NM_015636.3:c.784C>G	NP_056451.3:p.Leu262Val
NM_172195.3:c.847C>G	NP_751945.2:p.Leu283Val
XM_005264632.1:c.742C>G	XP_005264689.1:p.Leu248Val
XM_006712132.1:c.739C>G	XP_006712195.1:p.Leu247Val
XM_011533147.1:c.169C>G	XP_011531449.1:p.Leu57Val
NM_001318965.1:c.850C>G	NP_001305894.1:p.Leu284Val
NM_001318966.1:c.742C>G	NP_001305895.1:p.Leu248Val
NM_001318967.1:c.694C>G	NP_001305896.1:p.Leu232Val
NM_001318968.1:c.202C>G	NP_001305897.1:p.Leu68Val
NM_001318969.1:c.169C>G	NP_001305898.1:p.Leu57Val
XM_011533147.2:c.169C>G	XP_011531449.1:p.Leu57Val
NM_001034116.2:c.787C>G MANE Select	NP_001029288.1:p.Leu263Val
NM_001318965.2:c.850C>G	NP_001305894.1:p.Leu284Val
NM_001318966.2:c.742C>G	NP_001305895.1:p.Leu248Val
NM_001318967.2:c.694C>G	NP_001305896.1:p.Leu232Val
NM_001318968.2:c.202C>G	NP_001305897.1:p.Leu68Val
NM_001318969.2:c.169C>G	NP_001305898.1:p.Leu57Val
NM_015636.4:c.784C>G	NP_056451.3:p.Leu262Val
NM_172195.4:c.847C>G	NP_751945.2:p.Leu283Val