Canonical Allele Identifier: CA2171566077
Gene: EIF2AK4 HGNC NCBI

Linked Data

dbSNP Id: rs2034722144

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39977812_39977816del , CM000677.2:g.39977812_39977816del GRCh38
NC_000015.9:g.40270013_40270017del , CM000677.1:g.40270013_40270017del GRCh37
NC_000015.8:g.38057305_38057309del NCBI36
NG_034053.1:g.48689_48693del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263791.10:c.2250-266_2250-262del MANE Select ENSP00000263791.5:n.2250-266_2250-262del
ENST00000263791.9:c.2250-266_2250-262del ENSP00000263791.5:n.2250-266_2250-262del
ENST00000560855.5:c.1666-266_1666-262del
ENST00000624709.1:n.834_838del
NM_001013703.3:c.2250-266_2250-262del NP_001013725.2:n.2250-266_2250-262del
XM_005254392.1:c.2250-266_2250-262del XP_005254449.1:n.2250-266_2250-262del
XM_011521599.1:c.2250-266_2250-262del XP_011519901.1:n.2250-266_2250-262del
XM_011521600.1:c.2250-266_2250-262del XP_011519902.1:n.2250-266_2250-262del
XM_005254392.3:c.2250-266_2250-262del XP_005254449.1:n.2250-266_2250-262del
XM_011521599.2:c.2250-266_2250-262del XP_011519901.1:n.2250-266_2250-262del
XM_011521600.3:c.2250-266_2250-262del XP_011519902.1:n.2250-266_2250-262del
XM_017022219.2:c.2250-266_2250-262del XP_016877708.1:n.2250-266_2250-262del
NM_001013703.4:c.2250-266_2250-262del MANE Select NP_001013725.2:n.2250-266_2250-262del