Canonical Allele Identifier: CA576711309
Community Standard Title: NM_004722.4(AP4M1):c.544-186dup
Gene: AP4M1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100103906dup , CM000669.2:g.100103906dup GRCh38
NC_000007.13:g.99701529dup , CM000669.1:g.99701529dup GRCh37
NC_000007.12:g.99539465dup NCBI36
NG_016312.1:g.7400dup

Transcript Alleles

HGVS Amino-acid Change
NM_004722.4:c.544-186dup MANE Select NP_004713.2:n.544-186dup
ENST00000359593.9:c.544-186dup MANE Select ENSP00000352603.4:n.544-186dup
NM_001363671.1:c.565-186dup NP_001350600.1:n.565-186dup
NM_001363671.2:c.565-186dup NP_001350600.1:n.565-186dup
NM_004722.3:c.544-186dup NP_004713.2:n.544-186dup
ENST00000359593.8:c.544-186dup ENSP00000352603.4:n.544-186dup
ENST00000416938.5:c.500-186dup
ENST00000421755.5:c.544-186dup ENSP00000412185.1:n.544-186dup
ENST00000422582.5:c.160-186dup ENSP00000406676.1:n.160-186dup
ENST00000429084.5:c.565-186dup ENSP00000403663.1:n.565-186dup
ENST00000438383.5:c.340-186dup ENSP00000401613.1:n.340-186dup
ENST00000439416.5:c.412-186dup ENSP00000414286.1:n.412-186dup
ENST00000445208.5:c.*153-186dup ENSP00000400598.1:n.*153-186dup
ENST00000445295.2:c.544-186dup ENSP00000393723.2:n.544-186dup
ENST00000446007.5:c.544-186dup ENSP00000396928.1:n.544-186dup
ENST00000463195.5:n.618-186dup
ENST00000479916.1:n.126-186dup
ENST00000495154.2:n.803-186dup
ENST00000713591.1:c.544-186dup ENSP00000518888.1:n.544-186dup
XM_005250689.3:c.565-186dup XP_005250746.1:n.565-186dup
XM_005250689.4:c.565-186dup XP_005250746.1:n.565-186dup
XM_005250690.3:c.340-186dup XP_005250747.1:n.340-186dup
XM_005250690.4:c.340-186dup XP_005250747.1:n.340-186dup
XM_006716175.2:c.565-186dup XP_006716238.1:n.565-186dup
XM_006716175.4:c.565-186dup XP_006716238.1:n.565-186dup
XM_011516685.1:c.565-186dup XP_011514987.1:n.565-186dup
XM_011516686.1:c.160-186dup XP_011514988.1:n.160-186dup
XM_011516687.1:c.-65-186dup XP_011514989.1:n.-65-186dup
XM_017012790.2:c.160-186dup XP_016868279.1:n.160-186dup
XM_017012791.2:c.-65-186dup XP_016868280.1:n.-65-186dup
XM_024446995.1:c.544-186dup XP_024302763.1:n.544-186dup
XM_024446996.1:c.-65-186dup XP_024302764.1:n.-65-186dup