Canonical Allele Identifier: CA2627755675
Gene: EIF2AK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40016529_40016533del , CM000677.2:g.40016529_40016533del GRCh38
NC_000015.9:g.40308730_40308734del , CM000677.1:g.40308730_40308734del GRCh37
NC_000015.8:g.38096022_38096026del NCBI36
NG_034053.1:g.87406_87410del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263791.10:c.3787_3791del MANE Select ENSP00000263791.5:p.Gln1263GlyfsTer?
ENST00000263791.9:c.3787_3791del ENSP00000263791.5:p.Gln1263GlyfsTer?
ENST00000558557.1:n.923-579_923-575del
ENST00000558629.5:n.2704_2708del
ENST00000560855.5:c.3119_3123del
NM_001013703.3:c.3787_3791del NP_001013725.2:p.Gln1263GlyfsTer?
XM_005254392.1:c.3787_3791del XP_005254449.1:p.Gln1263GlyfsTer?
XM_011521599.1:c.3787_3791del XP_011519901.1:p.Gln1263GlyfsTer?
XM_011521600.1:c.3760-579_3760-575del XP_011519902.1:n.3760-579_3760-575del
XM_005254392.3:c.3787_3791del XP_005254449.1:p.Gln1263GlyfsTer?
XM_011521599.2:c.3787_3791del XP_011519901.1:p.Gln1263GlyfsTer?
XM_011521600.3:c.3760-579_3760-575del XP_011519902.1:n.3760-579_3760-575del
XM_017022219.2:c.3760-579_3760-575del XP_016877708.1:n.3760-579_3760-575del
NM_001013703.4:c.3787_3791del MANE Select NP_001013725.2:p.Gln1263GlyfsTer?