Canonical Allele Identifier: CA2171566211
Gene: EIF2AK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39978135_39978139delinsAAGTC , CM000677.2:g.39978135_39978139delinsAAGTC GRCh38
NC_000015.9:g.40270336_40270340delinsAAGTC , CM000677.1:g.40270336_40270340delinsAAGTC GRCh37
NC_000015.8:g.38057628_38057632delinsAAGTC NCBI36
NG_034053.1:g.49012_49016delinsAAGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263791.10:c.2307_2311delinsAAGTC MANE Select ENSP00000263791.5:p.Lys769=
ENST00000263791.9:c.2307_2311delinsAAGTC ENSP00000263791.5:p.Lys769=
ENST00000560855.5:c.1723_1727delinsAAGTC
ENST00000624709.1:n.1157_1161delinsAAGTC
NM_001013703.3:c.2307_2311delinsAAGTC NP_001013725.2:p.Lys769=
XM_005254392.1:c.2307_2311delinsAAGTC XP_005254449.1:p.Lys769=
XM_011521599.1:c.2307_2311delinsAAGTC XP_011519901.1:p.Lys769=
XM_011521600.1:c.2307_2311delinsAAGTC XP_011519902.1:p.Lys769=
XM_005254392.3:c.2307_2311delinsAAGTC XP_005254449.1:p.Lys769=
XM_011521599.2:c.2307_2311delinsAAGTC XP_011519901.1:p.Lys769=
XM_011521600.3:c.2307_2311delinsAAGTC XP_011519902.1:p.Lys769=
XM_017022219.2:c.2307_2311delinsAAGTC XP_016877708.1:p.Lys769=
NM_001013703.4:c.2307_2311delinsAAGTC MANE Select NP_001013725.2:p.Lys769=