Canonical Allele Identifier: CA2575675858

Gene: EIF2AK4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40016770_40016776del , CM000677.2:g.40016770_40016776del	GRCh38
NC_000015.9:g.40308971_40308977del , CM000677.1:g.40308971_40308977del	GRCh37
NC_000015.8:g.38096263_38096269del	NCBI36
NG_034053.1:g.87647_87653del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263791.10:c.3930+98_3930+104del MANE Select	ENSP00000263791.5:n.3930+98_3930+104del
ENST00000263791.9:c.3930+98_3930+104del	ENSP00000263791.5:n.3930+98_3930+104del
ENST00000558557.1:n.923-338_923-332del
ENST00000558629.5:n.2847+98_2847+104del
ENST00000560855.5:c.3262+98_3262+104del
NM_001013703.3:c.3930+98_3930+104del	NP_001013725.2:n.3930+98_3930+104del
XM_005254392.1:c.3930+98_3930+104del	XP_005254449.1:n.3930+98_3930+104del
XM_011521599.1:c.3930+98_3930+104del	XP_011519901.1:n.3930+98_3930+104del
XM_011521600.1:c.3760-338_3760-332del	XP_011519902.1:n.3760-338_3760-332del
XM_005254392.3:c.3930+98_3930+104del	XP_005254449.1:n.3930+98_3930+104del
XM_011521599.2:c.3930+98_3930+104del	XP_011519901.1:n.3930+98_3930+104del
XM_011521600.3:c.3760-338_3760-332del	XP_011519902.1:n.3760-338_3760-332del
XM_017022219.2:c.3760-338_3760-332del	XP_016877708.1:n.3760-338_3760-332del
NM_001013703.4:c.3930+98_3930+104del MANE Select	NP_001013725.2:n.3930+98_3930+104del