Canonical Allele Identifier: CA2695105336

Gene: MECP2

Linked Data

• gnomAD v4: X-154097551-A-AGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097551_154097552insGGC , CM000685.2:g.154097551_154097552insGGC	GRCh38
NC_000023.10:g.153363008_153363009insGGC , CM000685.1:g.153363008_153363009insGGC	GRCh37
NC_000023.9:g.153016202_153016203insGGC	NCBI36
NG_007107.2:g.44570_44571insGCC
NG_007107.3:g.44552_44553insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700484.1:n.22+52_22+53insGCC
ENST00000303391.11:c.-99+52_-99+53insGCC MANE Plus Clinical	ENSP00000301948.6:n.-99+52_-99+53insGCC
ENST00000453960.7:c.62+52_62+53insGCC MANE Select	ENSP00000395535.2:n.62+52_62+53insGCC
ENST00000676382.1:n.22+52_22+53insGCC
ENST00000303391.10:c.-99+52_-99+53insGCC	ENSP00000301948.6:n.-99+52_-99+53insGCC
ENST00000369957.5:c.-99+52_-99+53insGCC	ENSP00000358973.4:n.-99+52_-99+53insGCC
ENST00000407218.5:c.62+52_62+53insGCC	ENSP00000384865.2:n.62+52_62+53insGCC
ENST00000453960.6:c.62+52_62+53insGCC	ENSP00000395535.2:n.62+52_62+53insGCC
ENST00000619732.4:c.-99+52_-99+53insGCC	ENSP00000480973.1:n.-99+52_-99+53insGCC
ENST00000627864.1:n.77+52_77+53insGCC
ENST00000628176.2:c.-99+52_-99+53insGCC	ENSP00000486978.1:n.-99+52_-99+53insGCC
ENST00000631210.1:n.305+7229_305+7230insGCC
NM_001110792.1:c.62+52_62+53insGCC	NP_001104262.1:n.62+52_62+53insGCC
NM_001316337.1:c.-546+52_-546+53insGCC	NP_001303266.1:n.-546+52_-546+53insGCC
NM_004992.3:c.-99+52_-99+53insGCC	NP_004983.1:n.-99+52_-99+53insGCC
XM_005274682.3:c.-490+52_-490+53insGCC	XP_005274739.1:n.-490+52_-490+53insGCC
NM_001110792.2:c.62+52_62+53insGCC MANE Select	NP_001104262.1:n.62+52_62+53insGCC
NM_001316337.2:c.-546+52_-546+53insGCC	NP_001303266.1:n.-546+52_-546+53insGCC
NM_001369391.2:c.-841+52_-841+53insGCC	NP_001356320.1:n.-841+52_-841+53insGCC
NM_001369392.2:c.-490+52_-490+53insGCC	NP_001356321.1:n.-490+52_-490+53insGCC
NM_001369393.2:c.-366+52_-366+53insGCC	NP_001356322.1:n.-366+52_-366+53insGCC
NM_001386137.1:c.-771+52_-771+53insGCC	NP_001373066.1:n.-771+52_-771+53insGCC
NM_001386138.1:c.-659+52_-659+53insGCC	NP_001373067.1:n.-659+52_-659+53insGCC
NM_001386139.1:c.-535+52_-535+53insGCC	NP_001373068.1:n.-535+52_-535+53insGCC
NM_004992.4:c.-99+52_-99+53insGCC MANE Plus Clinical	NP_004983.1:n.-99+52_-99+53insGCC