Canonical Allele Identifier: CA270410
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143568
ClinVar RCV Id: RCV000133103
dbSNP Id: rs267608476

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154031408del , CM000685.2:g.154031408del GRCh38
NC_000023.10:g.153296859del , CM000685.1:g.153296859del GRCh37
NC_000023.9:g.152950053del NCBI36
NG_007107.2:g.110720del
NG_007107.3:g.110696del

Transcript Alleles

HGVS Amino-acid change
ENST00000303391.11:c.420del MANE Plus Clinical ENSP00000301948.6:p.Tyr141ThrfsTer5
ENST00000453960.7:c.456del MANE Select ENSP00000395535.2:p.Tyr153ThrfsTer5
ENST00000637917.1:c.53del
ENST00000303391.10:c.420del ENSP00000301948.6:p.Tyr141ThrfsTer5
ENST00000369957.5:c.*474del ENSP00000358973.4:n.*474del
ENST00000407218.5:c.456del ENSP00000384865.2:p.Tyr153ThrfsTer?
ENST00000453960.6:c.456del ENSP00000395535.2:p.Tyr153ThrfsTer5
ENST00000486506.5:n.2768del
ENST00000611468.1:c.408del ENSP00000479736.1:p.Tyr137ThrfsTer5
ENST00000619732.4:c.420del ENSP00000480973.1:p.Tyr141ThrfsTer5
ENST00000622433.4:c.408del ENSP00000484470.1:p.Tyr137ThrfsTer5
ENST00000628176.2:c.420del ENSP00000486978.1:p.Tyr141ThrfsTer?
NM_001110792.1:c.456del NP_001104262.1:p.Tyr153ThrfsTer5
NM_001316337.1:c.141del NP_001303266.1:p.Tyr48ThrfsTer5
NM_004992.3:c.420del NP_004983.1:p.Tyr141ThrfsTer5
XM_005274681.3:c.420del XP_005274738.1:p.Tyr141ThrfsTer5
XM_005274682.3:c.141del XP_005274739.1:p.Tyr48ThrfsTer5
XM_005274683.3:c.141del XP_005274740.1:p.Tyr48ThrfsTer5
XM_006724819.2:c.-141del XP_006724882.1:n.-141del
XM_011531166.1:c.141del XP_011529468.1:p.Tyr48ThrfsTer5
XM_006724819.3:c.-141del XP_006724882.1:n.-141del
XM_011531166.2:c.141del XP_011529468.1:p.Tyr48ThrfsTer5
XM_024452383.1:c.141del XP_024308151.1:p.Tyr48ThrfsTer5
XM_024452384.1:c.141del XP_024308152.1:p.Tyr48ThrfsTer5
NM_001110792.2:c.456del MANE Select NP_001104262.1:p.Tyr153ThrfsTer5
NM_001316337.2:c.141del NP_001303266.1:p.Tyr48ThrfsTer5
NM_001369391.2:c.141del NP_001356320.1:p.Tyr48ThrfsTer5
NM_001369392.2:c.141del NP_001356321.1:p.Tyr48ThrfsTer5
NM_001369393.2:c.141del NP_001356322.1:p.Tyr48ThrfsTer5
NM_001369394.1:c.141del NP_001356323.1:p.Tyr48ThrfsTer5
NM_001369394.2:c.141del NP_001356323.1:p.Tyr48ThrfsTer5
NM_001386137.1:c.-141del NP_001373066.1:n.-141del
NM_001386138.1:c.-141del NP_001373067.1:n.-141del
NM_001386139.1:c.-141del NP_001373068.1:n.-141del
NM_004992.4:c.420del MANE Plus Clinical NP_004983.1:p.Tyr141ThrfsTer5