Canonical Allele Identifier: CA346199408

Gene: EIF2B4

Linked Data

• MyVariant Identifiers: chr2:g.27590423G>C (hg19) ; chr2:g.27367556G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27367556G>C , CM000664.2:g.27367556G>C	GRCh38
NC_000002.11:g.27590423G>C , CM000664.1:g.27590423G>C	GRCh37
NC_000002.10:g.27443927G>C	NCBI36
NG_009305.1:g.7902C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.786C>G MANE Select	ENSP00000233552.6:p.Phe262Leu
ENST00000347454.8:c.786C>G	ENSP00000233552.5:p.Phe262Leu
ENST00000405940.6:c.*52C>G	ENSP00000384375.2:n.*52C>G
ENST00000417567.1:c.362C>G
ENST00000445933.6:c.783C>G	ENSP00000394397.2:p.Phe261Leu
ENST00000451130.6:c.846C>G	ENSP00000394869.2:p.Phe282Leu
ENST00000475582.5:n.2295C>G
ENST00000493344.6:c.849C>G	ENSP00000429323.1:p.Phe283Leu
ENST00000616081.4:c.777C>G	ENSP00000477710.1:p.Phe259Leu
ENST00000622434.4:c.*52C>G	ENSP00000479991.1:n.*52C>G
NM_001034116.1:c.786C>G	NP_001029288.1:p.Phe262Leu
NM_015636.3:c.783C>G	NP_056451.3:p.Phe261Leu
NM_172195.3:c.846C>G	NP_751945.2:p.Phe282Leu
XM_005264632.1:c.741C>G	XP_005264689.1:p.Phe247Leu
XM_006712132.1:c.738C>G	XP_006712195.1:p.Phe246Leu
XM_011533147.1:c.168C>G	XP_011531449.1:p.Phe56Leu
NM_001318965.1:c.849C>G	NP_001305894.1:p.Phe283Leu
NM_001318966.1:c.741C>G	NP_001305895.1:p.Phe247Leu
NM_001318967.1:c.693C>G	NP_001305896.1:p.Phe231Leu
NM_001318968.1:c.201C>G	NP_001305897.1:p.Phe67Leu
NM_001318969.1:c.168C>G	NP_001305898.1:p.Phe56Leu
XM_011533147.2:c.168C>G	XP_011531449.1:p.Phe56Leu
NM_001034116.2:c.786C>G MANE Select	NP_001029288.1:p.Phe262Leu
NM_001318965.2:c.849C>G	NP_001305894.1:p.Phe283Leu
NM_001318966.2:c.741C>G	NP_001305895.1:p.Phe247Leu
NM_001318967.2:c.693C>G	NP_001305896.1:p.Phe231Leu
NM_001318968.2:c.201C>G	NP_001305897.1:p.Phe67Leu
NM_001318969.2:c.168C>G	NP_001305898.1:p.Phe56Leu
NM_015636.4:c.783C>G	NP_056451.3:p.Phe261Leu
NM_172195.4:c.846C>G	NP_751945.2:p.Phe282Leu