Canonical Allele Identifier: CA2466594785

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097639C= , CM000685.2:g.154097639C=	GRCh38
NC_000023.10:g.153363096C= , CM000685.1:g.153363096C=	GRCh37
NC_000023.9:g.153016290C=	NCBI36
NG_007107.2:g.44483G=
NG_007107.3:g.44465G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303391.11:c.-134G= MANE Plus Clinical	ENSP00000301948.6:n.-134G=
ENST00000453960.7:c.27G= MANE Select	ENSP00000395535.2:p.Pro9=
ENST00000303391.10:c.-134G=	ENSP00000301948.6:n.-134G=
ENST00000369957.5:c.-134G=	ENSP00000358973.4:n.-134G=
ENST00000407218.5:c.27G=	ENSP00000384865.2:p.Pro9=
ENST00000453960.6:c.27G=	ENSP00000395535.2:p.Pro9=
ENST00000619732.4:c.-134G=	ENSP00000480973.1:n.-134G=
ENST00000627864.1:n.42G=
ENST00000628176.2:c.-134G=	ENSP00000486978.1:n.-134G=
ENST00000631210.1:n.305+7142G=
NM_001110792.1:c.27G=	NP_001104262.1:p.Pro9=
NM_001316337.1:c.-581G=	NP_001303266.1:n.-581G=
NM_004992.3:c.-134G=	NP_004983.1:n.-134G=
XM_005274682.3:c.-525G=	XP_005274739.1:n.-525G=
NM_001110792.2:c.27G= MANE Select	NP_001104262.1:p.Pro9=
NM_001316337.2:c.-581G=	NP_001303266.1:n.-581G=
NM_001369391.2:c.-876G=	NP_001356320.1:n.-876G=
NM_001369392.2:c.-525G=	NP_001356321.1:n.-525G=
NM_001369393.2:c.-401G=	NP_001356322.1:n.-401G=
NM_001386137.1:c.-806G=	NP_001373066.1:n.-806G=
NM_001386138.1:c.-694G=	NP_001373067.1:n.-694G=
NM_001386139.1:c.-570G=	NP_001373068.1:n.-570G=
NM_004992.4:c.-134G= MANE Plus Clinical	NP_004983.1:n.-134G=