Canonical Allele Identifier: CA2499737281
Gene: MECP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097560_154097563del , CM000685.2:g.154097560_154097563del GRCh38
NC_000023.10:g.153363017_153363020del , CM000685.1:g.153363017_153363020del GRCh37
NC_000023.9:g.153016211_153016214del NCBI36
NG_007107.2:g.44561_44564del
NG_007107.3:g.44543_44546del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700484.1:n.22+43_22+46del
ENST00000303391.11:c.-99+43_-99+46del MANE Plus Clinical ENSP00000301948.6:n.-99+43_-99+46del
ENST00000453960.7:c.62+43_62+46del MANE Select ENSP00000395535.2:n.62+43_62+46del
ENST00000676382.1:n.22+43_22+46del
ENST00000303391.10:c.-99+43_-99+46del ENSP00000301948.6:n.-99+43_-99+46del
ENST00000369957.5:c.-99+43_-99+46del ENSP00000358973.4:n.-99+43_-99+46del
ENST00000407218.5:c.62+43_62+46del ENSP00000384865.2:n.62+43_62+46del
ENST00000453960.6:c.62+43_62+46del ENSP00000395535.2:n.62+43_62+46del
ENST00000619732.4:c.-99+43_-99+46del ENSP00000480973.1:n.-99+43_-99+46del
ENST00000627864.1:n.77+43_77+46del
ENST00000628176.2:c.-99+43_-99+46del ENSP00000486978.1:n.-99+43_-99+46del
ENST00000631210.1:n.305+7220_305+7223del
NM_001110792.1:c.62+43_62+46del NP_001104262.1:n.62+43_62+46del
NM_001316337.1:c.-546+43_-546+46del NP_001303266.1:n.-546+43_-546+46del
NM_004992.3:c.-99+43_-99+46del NP_004983.1:n.-99+43_-99+46del
XM_005274682.3:c.-490+43_-490+46del XP_005274739.1:n.-490+43_-490+46del
NM_001110792.2:c.62+43_62+46del MANE Select NP_001104262.1:n.62+43_62+46del
NM_001316337.2:c.-546+43_-546+46del NP_001303266.1:n.-546+43_-546+46del
NM_001369391.2:c.-841+43_-841+46del NP_001356320.1:n.-841+43_-841+46del
NM_001369392.2:c.-490+43_-490+46del NP_001356321.1:n.-490+43_-490+46del
NM_001369393.2:c.-366+43_-366+46del NP_001356322.1:n.-366+43_-366+46del
NM_001386137.1:c.-771+43_-771+46del NP_001373066.1:n.-771+43_-771+46del
NM_001386138.1:c.-659+43_-659+46del NP_001373067.1:n.-659+43_-659+46del
NM_001386139.1:c.-535+43_-535+46del NP_001373068.1:n.-535+43_-535+46del
NM_004992.4:c.-99+43_-99+46del MANE Plus Clinical NP_004983.1:n.-99+43_-99+46del