Canonical Allele Identifier: CA489666998

Gene: EIF2AK4

Linked Data

• MyVariant Identifiers: chr15:g.40313141C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40020940C>G , CM000677.2:g.40020940C>G	GRCh38
NC_000015.9:g.40313141C>G , CM000677.1:g.40313141C>G	GRCh37
NC_000015.8:g.38100433C>G	NCBI36
NG_034053.1:g.91817C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263791.10:c.4215C>G MANE Select	ENSP00000263791.5:p.Gly1405=
ENST00000263791.9:c.4215C>G	ENSP00000263791.5:p.Gly1405=
ENST00000558557.1:n.1207C>G
ENST00000558629.5:n.3132C>G
ENST00000558743.1:n.415C>G
ENST00000560855.5:c.3547C>G
NM_001013703.3:c.4215C>G	NP_001013725.2:p.Gly1405=
XM_005254392.1:c.4215C>G	XP_005254449.1:p.Gly1405=
XM_011521599.1:c.4215C>G	XP_011519901.1:p.Gly1405=
XM_011521600.1:c.4044C>G	XP_011519902.1:p.Gly1348=
XM_005254392.3:c.4215C>G	XP_005254449.1:p.Gly1405=
XM_011521599.2:c.4215C>G	XP_011519901.1:p.Gly1405=
XM_011521600.3:c.4044C>G	XP_011519902.1:p.Gly1348=
XM_017022219.2:c.4044C>G	XP_016877708.1:p.Gly1348=
NM_001013703.4:c.4215C>G MANE Select	NP_001013725.2:p.Gly1405=