Canonical Allele Identifier: CA270212
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143353
ClinVar RCV Id: RCV000132879 RCV002345447
dbSNP Id: rs267608576
MyVariant Identifiers: chrX:g.153296124_153296127del (hg19) chrX:g.154030673_154030676del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154030676_154030679del , CM000685.2:g.154030676_154030679del GRCh38
NC_000023.10:g.153296127_153296130del , CM000685.1:g.153296127_153296130del GRCh37
NC_000023.9:g.152949321_152949324del NCBI36
NG_007107.2:g.111452_111455del
NG_007107.3:g.111428_111431del

Transcript Alleles

HGVS Amino-acid change
ENST00000303391.11:c.1152_1155del MANE Plus Clinical ENSP00000301948.6:p.Pro385CysfsTer23
ENST00000453960.7:c.1188_1191del MANE Select ENSP00000395535.2:p.Pro397CysfsTer23
ENST00000303391.10:c.1152_1155del ENSP00000301948.6:p.Pro385CysfsTer23
ENST00000407218.5:c.*524_*527del ENSP00000384865.2:n.*524_*527del
ENST00000453960.6:c.1188_1191del ENSP00000395535.2:p.Pro397CysfsTer23
ENST00000619732.4:c.1152_1155del ENSP00000480973.1:p.Pro385CysfsTer23
ENST00000628176.2:c.*524_*527del ENSP00000486978.1:n.*524_*527del
NM_001110792.1:c.1188_1191del NP_001104262.1:p.Pro397CysfsTer23
NM_001316337.1:c.873_876del NP_001303266.1:p.Pro292CysfsTer23
NM_004992.3:c.1152_1155del NP_004983.1:p.Pro385CysfsTer23
XM_005274681.3:c.1152_1155del XP_005274738.1:p.Pro385CysfsTer23
XM_005274682.3:c.873_876del XP_005274739.1:p.Pro292CysfsTer23
XM_005274683.3:c.873_876del XP_005274740.1:p.Pro292CysfsTer23
XM_006724819.2:c.483_486del XP_006724882.1:p.Pro162CysfsTer23
XM_011531166.1:c.873_876del XP_011529468.1:p.Pro292CysfsTer23
XM_006724819.3:c.483_486del XP_006724882.1:p.Pro162CysfsTer23
XM_011531166.2:c.873_876del XP_011529468.1:p.Pro292CysfsTer23
XM_024452383.1:c.873_876del XP_024308151.1:p.Pro292CysfsTer23
XM_024452384.1:c.873_876del XP_024308152.1:p.Pro292CysfsTer23
NM_001110792.2:c.1188_1191del MANE Select NP_001104262.1:p.Pro397CysfsTer23
NM_001316337.2:c.873_876del NP_001303266.1:p.Pro292CysfsTer23
NM_001369391.2:c.873_876del NP_001356320.1:p.Pro292CysfsTer23
NM_001369392.2:c.873_876del NP_001356321.1:p.Pro292CysfsTer23
NM_001369393.2:c.873_876del NP_001356322.1:p.Pro292CysfsTer23
NM_001369394.1:c.873_876del NP_001356323.1:p.Pro292CysfsTer23
NM_001369394.2:c.873_876del NP_001356323.1:p.Pro292CysfsTer23
NM_001386137.1:c.483_486del NP_001373066.1:p.Pro162CysfsTer23
NM_001386138.1:c.483_486del NP_001373067.1:p.Pro162CysfsTer23
NM_001386139.1:c.483_486del NP_001373068.1:p.Pro162CysfsTer23
NM_004992.4:c.1152_1155del MANE Plus Clinical NP_004983.1:p.Pro385CysfsTer23
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