Canonical Allele Identifier: CA2466594762

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097610T= , CM000685.2:g.154097610T=	GRCh38
NC_000023.10:g.153363067T= , CM000685.1:g.153363067T=	GRCh37
NC_000023.9:g.153016261T=	NCBI36
NG_007107.2:g.44512A=
NG_007107.3:g.44494A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700484.1:n.16A=
ENST00000303391.11:c.-105A= MANE Plus Clinical	ENSP00000301948.6:n.-105A=
ENST00000453960.7:c.56A= MANE Select	ENSP00000395535.2:p.Glu19=
ENST00000676382.1:n.16A=
ENST00000303391.10:c.-105A=	ENSP00000301948.6:n.-105A=
ENST00000369957.5:c.-105A=	ENSP00000358973.4:n.-105A=
ENST00000407218.5:c.56A=	ENSP00000384865.2:p.Glu19=
ENST00000453960.6:c.56A=	ENSP00000395535.2:p.Glu19=
ENST00000619732.4:c.-105A=	ENSP00000480973.1:n.-105A=
ENST00000627864.1:n.71A=
ENST00000628176.2:c.-105A=	ENSP00000486978.1:n.-105A=
ENST00000631210.1:n.305+7171A=
NM_001110792.1:c.56A=	NP_001104262.1:p.Glu19=
NM_001316337.1:c.-552A=	NP_001303266.1:n.-552A=
NM_004992.3:c.-105A=	NP_004983.1:n.-105A=
XM_005274682.3:c.-496A=	XP_005274739.1:n.-496A=
NM_001110792.2:c.56A= MANE Select	NP_001104262.1:p.Glu19=
NM_001316337.2:c.-552A=	NP_001303266.1:n.-552A=
NM_001369391.2:c.-847A=	NP_001356320.1:n.-847A=
NM_001369392.2:c.-496A=	NP_001356321.1:n.-496A=
NM_001369393.2:c.-372A=	NP_001356322.1:n.-372A=
NM_001386137.1:c.-777A=	NP_001373066.1:n.-777A=
NM_001386138.1:c.-665A=	NP_001373067.1:n.-665A=
NM_001386139.1:c.-541A=	NP_001373068.1:n.-541A=
NM_004992.4:c.-105A= MANE Plus Clinical	NP_004983.1:n.-105A=