Canonical Allele Identifier: CA2695237641
Gene: MECP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154032440_154032444del , CM000685.2:g.154032440_154032444del GRCh38
NC_000023.10:g.153297891_153297895del , CM000685.1:g.153297891_153297895del GRCh37
NC_000023.9:g.152951085_152951089del NCBI36
NG_007107.2:g.109684_109688del
NG_007107.3:g.109660_109664del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.140_144del MANE Plus Clinical ENSP00000301948.6:p.Gln47LeufsTer7
ENST00000453960.7:c.176_180del MANE Select ENSP00000395535.2:p.Gln59LeufsTer7
ENST00000303391.10:c.140_144del ENSP00000301948.6:p.Gln47LeufsTer7
ENST00000369957.5:c.*194_*198del ENSP00000358973.4:n.*194_*198del
ENST00000407218.5:c.176_180del ENSP00000384865.2:p.Gln59LeufsTer7
ENST00000415944.3:c.140_144del ENSP00000416267.1:p.Gln47LeufsTer?
ENST00000453960.6:c.176_180del ENSP00000395535.2:p.Gln59LeufsTer7
ENST00000460227.4:n.1289_1293del
ENST00000463644.5:n.1079_1083del
ENST00000481807.3:n.426_430del
ENST00000486506.5:n.2488_2492del
ENST00000488293.4:n.1189_1193del
ENST00000496908.5:n.271_275del
ENST00000611468.1:c.128_132del ENSP00000479736.1:p.Gln43LeufsTer7
ENST00000619732.4:c.140_144del ENSP00000480973.1:p.Gln47LeufsTer7
ENST00000622433.4:c.128_132del ENSP00000484470.1:p.Gln43LeufsTer7
ENST00000628176.2:c.140_144del ENSP00000486978.1:p.Gln47LeufsTer7
ENST00000631210.1:n.419_423del
NM_001110792.1:c.176_180del NP_001104262.1:p.Gln59LeufsTer7
NM_001316337.1:c.-140_-136del NP_001303266.1:n.-140_-136del
NM_004992.3:c.140_144del NP_004983.1:p.Gln47LeufsTer7
XM_005274681.3:c.140_144del XP_005274738.1:p.Gln47LeufsTer7
XM_005274682.3:c.-140_-136del XP_005274739.1:n.-140_-136del
XM_005274683.3:c.-140_-136del XP_005274740.1:n.-140_-136del
XM_011531166.1:c.-140_-136del XP_011529468.1:n.-140_-136del
XM_006724819.3:c.-421_-417del XP_006724882.1:n.-421_-417del
XM_011531166.2:c.-140_-136del XP_011529468.1:n.-140_-136del
XM_024452383.1:c.-140_-136del XP_024308151.1:n.-140_-136del
XM_024452384.1:c.-140_-136del XP_024308152.1:n.-140_-136del
NM_001110792.2:c.176_180del MANE Select NP_001104262.1:p.Gln59LeufsTer7
NM_001316337.2:c.-140_-136del NP_001303266.1:n.-140_-136del
NM_001369391.2:c.-140_-136del NP_001356320.1:n.-140_-136del
NM_001369392.2:c.-140_-136del NP_001356321.1:n.-140_-136del
NM_001369393.2:c.-140_-136del NP_001356322.1:n.-140_-136del
NM_001369394.1:c.-140_-136del NP_001356323.1:n.-140_-136del
NM_001369394.2:c.-140_-136del NP_001356323.1:n.-140_-136del
NM_001386137.1:c.-421_-417del NP_001373066.1:n.-421_-417del
NM_001386138.1:c.-421_-417del NP_001373067.1:n.-421_-417del
NM_001386139.1:c.-421_-417del NP_001373068.1:n.-421_-417del
NM_004992.4:c.140_144del MANE Plus Clinical NP_004983.1:p.Gln47LeufsTer7