Canonical Allele Identifier: CA2176626641
Gene: AP4E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50912171C= , CM000677.2:g.50912171C= GRCh38
NC_000015.9:g.51204368C= , CM000677.1:g.51204368C= GRCh37
NC_000015.8:g.48991660C= NCBI36
NG_031875.1:g.8500C=
NG_031875.2:g.8500C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261842.10:c.222+22C= MANE Select ENSP00000261842.5:n.222+22C=
ENST00000261842.9:c.222+22C= ENSP00000261842.5:n.222+22C=
ENST00000558439.5:c.222+22C= ENSP00000452712.1:n.222+22C=
ENST00000560508.1:c.-27+22C= ENSP00000452976.1:n.-27+22C=
ENST00000561393.5:c.-27+22C= ENSP00000452711.1:n.-27+22C=
ENST00000561441.5:c.222+22C= ENSP00000453112.1:n.222+22C=
NM_001252127.1:c.-27+22C= NP_001239056.1:n.-27+22C=
NM_007347.4:c.222+22C= NP_031373.2:n.222+22C=
XM_005254264.2:c.-4+22C= XP_005254321.1:n.-4+22C=
XM_006720447.2:c.-4+22C= XP_006720510.1:n.-4+22C=
XM_011521409.1:c.-1219+22C= XP_011519711.1:n.-1219+22C=
XM_005254264.4:c.-4+22C= XP_005254321.1:n.-4+22C=
XM_006720447.4:c.-4+22C= XP_006720510.1:n.-4+22C=
XM_017022042.2:c.-749+22C= XP_016877531.1:n.-749+22C=
XR_001751183.1:n.329+22C=
XR_001751184.1:n.329+22C=
XR_001751185.1:n.329+22C=
NM_007347.5:c.222+22C= MANE Select NP_031373.2:n.222+22C=
NM_001252127.2:c.-27+22C= NP_001239056.1:n.-27+22C=