Canonical Allele Identifier: CA645289947
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs1557137975

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154032479_154032481del , CM000685.2:g.154032479_154032481del GRCh38
NC_000023.10:g.153297930_153297932del , CM000685.1:g.153297930_153297932del GRCh37
NC_000023.9:g.152951124_152951126del NCBI36
NG_007107.2:g.109649_109651del
NG_007107.3:g.109625_109627del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.105_107del MANE Plus Clinical ENSP00000301948.6:p.Lys36del
ENST00000453960.7:c.141_143del MANE Select ENSP00000395535.2:p.Lys48del
ENST00000611468.2:n.353_355del
ENST00000630151.2:c.105_107del ENSP00000486089.1:p.Lys36del
ENST00000637533.1:n.136_138del
ENST00000676382.1:n.298_300del
ENST00000303391.10:c.105_107del ENSP00000301948.6:p.Lys36del
ENST00000369957.5:c.*159_*161del ENSP00000358973.4:n.*159_*161del
ENST00000407218.5:c.141_143del ENSP00000384865.2:p.Lys48del
ENST00000415944.3:c.105_107del ENSP00000416267.1:p.Lys36del
ENST00000453960.6:c.141_143del ENSP00000395535.2:p.Lys48del
ENST00000460227.4:n.1254_1256del
ENST00000463644.5:n.1044_1046del
ENST00000481807.3:n.391_393del
ENST00000486506.5:n.2453_2455del
ENST00000488293.4:n.1154_1156del
ENST00000496908.5:n.236_238del
ENST00000611468.1:c.93_95del ENSP00000479736.1:p.Lys32del
ENST00000619732.4:c.105_107del ENSP00000480973.1:p.Lys36del
ENST00000622433.4:c.93_95del ENSP00000484470.1:p.Lys32del
ENST00000625300.1:n.330_332del
ENST00000626422.2:n.815_817del
ENST00000628176.2:c.105_107del ENSP00000486978.1:p.Lys36del
ENST00000630151.1:c.105_107del ENSP00000486089.1:p.Lys36del
ENST00000631210.1:n.384_386del
NM_001110792.1:c.141_143del NP_001104262.1:p.Lys48del
NM_001316337.1:c.-175_-173del NP_001303266.1:n.-175_-173del
NM_004992.3:c.105_107del NP_004983.1:p.Lys36del
XM_005274681.3:c.105_107del XP_005274738.1:p.Lys36del
XM_005274682.3:c.-175_-173del XP_005274739.1:n.-175_-173del
XM_005274683.3:c.-175_-173del XP_005274740.1:n.-175_-173del
XM_011531166.1:c.-175_-173del XP_011529468.1:n.-175_-173del
XM_006724819.3:c.-456_-454del XP_006724882.1:n.-456_-454del
XM_011531166.2:c.-175_-173del XP_011529468.1:n.-175_-173del
XM_024452383.1:c.-175_-173del XP_024308151.1:n.-175_-173del
XM_024452384.1:c.-175_-173del XP_024308152.1:n.-175_-173del
NM_001110792.2:c.141_143del MANE Select NP_001104262.1:p.Lys48del
NM_001316337.2:c.-175_-173del NP_001303266.1:n.-175_-173del
NM_001369391.2:c.-175_-173del NP_001356320.1:n.-175_-173del
NM_001369392.2:c.-175_-173del NP_001356321.1:n.-175_-173del
NM_001369393.2:c.-175_-173del NP_001356322.1:n.-175_-173del
NM_001369394.1:c.-175_-173del NP_001356323.1:n.-175_-173del
NM_001369394.2:c.-175_-173del NP_001356323.1:n.-175_-173del
NM_001386137.1:c.-456_-454del NP_001373066.1:n.-456_-454del
NM_001386138.1:c.-456_-454del NP_001373067.1:n.-456_-454del
NM_001386139.1:c.-456_-454del NP_001373068.1:n.-456_-454del
NM_004992.4:c.105_107del MANE Plus Clinical NP_004983.1:p.Lys36del