Canonical Allele Identifier: CA268738488

Gene: EIF2AK4

Linked Data

• dbSNP Id: rs111296603
• MyVariant Identifiers: chr15:g.40270214_40270215insG (hg19) ; chr15:g.39978013_39978014insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.39978013_39978014insG , CM000677.2:g.39978013_39978014insG	GRCh38
NC_000015.9:g.40270214_40270215insG , CM000677.1:g.40270214_40270215insG	GRCh37
NC_000015.8:g.38057506_38057507insG	NCBI36
NG_034053.1:g.48890_48891insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263791.10:c.2250-65_2250-64insG MANE Select	ENSP00000263791.5:n.2250-65_2250-64insG
ENST00000263791.9:c.2250-65_2250-64insG	ENSP00000263791.5:n.2250-65_2250-64insG
ENST00000560855.5:c.1666-65_1666-64insG
ENST00000624709.1:n.1035_1036insG
NM_001013703.3:c.2250-65_2250-64insG	NP_001013725.2:n.2250-65_2250-64insG
XM_005254392.1:c.2250-65_2250-64insG	XP_005254449.1:n.2250-65_2250-64insG
XM_011521599.1:c.2250-65_2250-64insG	XP_011519901.1:n.2250-65_2250-64insG
XM_011521600.1:c.2250-65_2250-64insG	XP_011519902.1:n.2250-65_2250-64insG
XM_005254392.3:c.2250-65_2250-64insG	XP_005254449.1:n.2250-65_2250-64insG
XM_011521599.2:c.2250-65_2250-64insG	XP_011519901.1:n.2250-65_2250-64insG
XM_011521600.3:c.2250-65_2250-64insG	XP_011519902.1:n.2250-65_2250-64insG
XM_017022219.2:c.2250-65_2250-64insG	XP_016877708.1:n.2250-65_2250-64insG
NM_001013703.4:c.2250-65_2250-64insG MANE Select	NP_001013725.2:n.2250-65_2250-64insG