Canonical Allele Identifier: CA2627751658
Gene: EIF2AK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39977844_39977845insTG , CM000677.2:g.39977844_39977845insTG GRCh38
NC_000015.9:g.40270045_40270046insTG , CM000677.1:g.40270045_40270046insTG GRCh37
NC_000015.8:g.38057337_38057338insTG NCBI36
NG_034053.1:g.48721_48722insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263791.10:c.2250-234_2250-233insTG MANE Select ENSP00000263791.5:n.2250-234_2250-233insTG
ENST00000263791.9:c.2250-234_2250-233insTG ENSP00000263791.5:n.2250-234_2250-233insTG
ENST00000560855.5:c.1666-234_1666-233insTG
ENST00000624709.1:n.866_867insTG
NM_001013703.3:c.2250-234_2250-233insTG NP_001013725.2:n.2250-234_2250-233insTG
XM_005254392.1:c.2250-234_2250-233insTG XP_005254449.1:n.2250-234_2250-233insTG
XM_011521599.1:c.2250-234_2250-233insTG XP_011519901.1:n.2250-234_2250-233insTG
XM_011521600.1:c.2250-234_2250-233insTG XP_011519902.1:n.2250-234_2250-233insTG
XM_005254392.3:c.2250-234_2250-233insTG XP_005254449.1:n.2250-234_2250-233insTG
XM_011521599.2:c.2250-234_2250-233insTG XP_011519901.1:n.2250-234_2250-233insTG
XM_011521600.3:c.2250-234_2250-233insTG XP_011519902.1:n.2250-234_2250-233insTG
XM_017022219.2:c.2250-234_2250-233insTG XP_016877708.1:n.2250-234_2250-233insTG
NM_001013703.4:c.2250-234_2250-233insTG MANE Select NP_001013725.2:n.2250-234_2250-233insTG