Canonical Allele Identifier: CA199485
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 189754
dbSNP Id: rs1557134946

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154030432_154030671del , CM000685.2:g.154030432_154030671del GRCh38
NC_000023.10:g.153295883_153296122del , CM000685.1:g.153295883_153296122del GRCh37
NC_000023.9:g.152949077_152949316del NCBI36
NG_007107.2:g.111461_111700del
NG_007107.3:g.111437_111676del

Transcript Alleles

HGVS Amino-acid change
ENST00000303391.11:c.1161_1400del MANE Plus Clinical ENSP00000301948.6:p.Pro388_Pro467del
ENST00000453960.7:c.1197_1436del MANE Select ENSP00000395535.2:p.Pro400_Pro479del
ENST00000303391.10:c.1161_1400del ENSP00000301948.6:p.Pro388_Pro467del
ENST00000453960.6:c.1197_1436del ENSP00000395535.2:p.Pro400_Pro479del
ENST00000619732.4:c.1161_1400del ENSP00000480973.1:p.Pro388_Pro467del
ENST00000628176.2:c.*533_*772del ENSP00000486978.1:n.*533_*772del
NM_001110792.1:c.1197_1436del NP_001104262.1:p.Pro400_Pro479del
NM_001316337.1:c.882_1121del NP_001303266.1:p.Pro295_Pro374del
NM_004992.3:c.1161_1400del NP_004983.1:p.Pro388_Pro467del
XM_005274681.3:c.1161_1400del XP_005274738.1:p.Pro388_Pro467del
XM_005274682.3:c.882_1121del XP_005274739.1:p.Pro295_Pro374del
XM_005274683.3:c.882_1121del XP_005274740.1:p.Pro295_Pro374del
XM_006724819.2:c.492_731del XP_006724882.1:p.Pro165_Pro244del
XM_011531166.1:c.882_1121del XP_011529468.1:p.Pro295_Pro374del
XM_006724819.3:c.492_731del XP_006724882.1:p.Pro165_Pro244del
XM_011531166.2:c.882_1121del XP_011529468.1:p.Pro295_Pro374del
XM_024452383.1:c.882_1121del XP_024308151.1:p.Pro295_Pro374del
XM_024452384.1:c.882_1121del XP_024308152.1:p.Pro295_Pro374del
NM_001110792.2:c.1197_1436del MANE Select NP_001104262.1:p.Pro400_Pro479del
NM_001316337.2:c.882_1121del NP_001303266.1:p.Pro295_Pro374del
NM_001369391.2:c.882_1121del NP_001356320.1:p.Pro295_Pro374del
NM_001369392.2:c.882_1121del NP_001356321.1:p.Pro295_Pro374del
NM_001369393.2:c.882_1121del NP_001356322.1:p.Pro295_Pro374del
NM_001369394.1:c.882_1121del NP_001356323.1:p.Pro295_Pro374del
NM_001369394.2:c.882_1121del NP_001356323.1:p.Pro295_Pro374del
NM_001386137.1:c.492_731del NP_001373066.1:p.Pro165_Pro244del
NM_001386138.1:c.492_731del NP_001373067.1:p.Pro165_Pro244del
NM_001386139.1:c.492_731del NP_001373068.1:p.Pro165_Pro244del
NM_004992.4:c.1161_1400del MANE Plus Clinical NP_004983.1:p.Pro388_Pro467del