Canonical Allele Identifier: CA2627751582
Gene: EIF2AK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39977751_39977752insAGC , CM000677.2:g.39977751_39977752insAGC GRCh38
NC_000015.9:g.40269952_40269953insAGC , CM000677.1:g.40269952_40269953insAGC GRCh37
NC_000015.8:g.38057244_38057245insAGC NCBI36
NG_034053.1:g.48628_48629insAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263791.10:c.2250-327_2250-326insAGC MANE Select ENSP00000263791.5:n.2250-327_2250-326insAGC
ENST00000263791.9:c.2250-327_2250-326insAGC ENSP00000263791.5:n.2250-327_2250-326insAGC
ENST00000560855.5:c.1666-327_1666-326insAGC
ENST00000624709.1:n.773_774insAGC
NM_001013703.3:c.2250-327_2250-326insAGC NP_001013725.2:n.2250-327_2250-326insAGC
XM_005254392.1:c.2250-327_2250-326insAGC XP_005254449.1:n.2250-327_2250-326insAGC
XM_011521599.1:c.2250-327_2250-326insAGC XP_011519901.1:n.2250-327_2250-326insAGC
XM_011521600.1:c.2250-327_2250-326insAGC XP_011519902.1:n.2250-327_2250-326insAGC
XM_005254392.3:c.2250-327_2250-326insAGC XP_005254449.1:n.2250-327_2250-326insAGC
XM_011521599.2:c.2250-327_2250-326insAGC XP_011519901.1:n.2250-327_2250-326insAGC
XM_011521600.3:c.2250-327_2250-326insAGC XP_011519902.1:n.2250-327_2250-326insAGC
XM_017022219.2:c.2250-327_2250-326insAGC XP_016877708.1:n.2250-327_2250-326insAGC
NM_001013703.4:c.2250-327_2250-326insAGC MANE Select NP_001013725.2:n.2250-327_2250-326insAGC