Canonical Allele Identifier: CA2508972196

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097591_154097592del , CM000685.2:g.154097591_154097592del	GRCh38
NC_000023.10:g.153363048_153363049del , CM000685.1:g.153363048_153363049del	GRCh37
NC_000023.9:g.153016242_153016243del	NCBI36
NG_007107.2:g.44531_44532del
NG_007107.3:g.44513_44514del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700484.1:n.22+13_22+14del
ENST00000303391.11:c.-99+13_-99+14del MANE Plus Clinical	ENSP00000301948.6:n.-99+13_-99+14del
ENST00000453960.7:c.62+13_62+14del MANE Select	ENSP00000395535.2:n.62+13_62+14del
ENST00000676382.1:n.22+13_22+14del
ENST00000303391.10:c.-99+13_-99+14del	ENSP00000301948.6:n.-99+13_-99+14del
ENST00000369957.5:c.-99+13_-99+14del	ENSP00000358973.4:n.-99+13_-99+14del
ENST00000407218.5:c.62+13_62+14del	ENSP00000384865.2:n.62+13_62+14del
ENST00000453960.6:c.62+13_62+14del	ENSP00000395535.2:n.62+13_62+14del
ENST00000619732.4:c.-99+13_-99+14del	ENSP00000480973.1:n.-99+13_-99+14del
ENST00000627864.1:n.77+13_77+14del
ENST00000628176.2:c.-99+13_-99+14del	ENSP00000486978.1:n.-99+13_-99+14del
ENST00000631210.1:n.305+7190_305+7191del
NM_001110792.1:c.62+13_62+14del	NP_001104262.1:n.62+13_62+14del
NM_001316337.1:c.-546+13_-546+14del	NP_001303266.1:n.-546+13_-546+14del
NM_004992.3:c.-99+13_-99+14del	NP_004983.1:n.-99+13_-99+14del
XM_005274682.3:c.-490+13_-490+14del	XP_005274739.1:n.-490+13_-490+14del
NM_001110792.2:c.62+13_62+14del MANE Select	NP_001104262.1:n.62+13_62+14del
NM_001316337.2:c.-546+13_-546+14del	NP_001303266.1:n.-546+13_-546+14del
NM_001369391.2:c.-841+13_-841+14del	NP_001356320.1:n.-841+13_-841+14del
NM_001369392.2:c.-490+13_-490+14del	NP_001356321.1:n.-490+13_-490+14del
NM_001369393.2:c.-366+13_-366+14del	NP_001356322.1:n.-366+13_-366+14del
NM_001386137.1:c.-771+13_-771+14del	NP_001373066.1:n.-771+13_-771+14del
NM_001386138.1:c.-659+13_-659+14del	NP_001373067.1:n.-659+13_-659+14del
NM_001386139.1:c.-535+13_-535+14del	NP_001373068.1:n.-535+13_-535+14del
NM_004992.4:c.-99+13_-99+14del MANE Plus Clinical	NP_004983.1:n.-99+13_-99+14del