Canonical Allele Identifier: CA2466594771

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097619C= , CM000685.2:g.154097619C=	GRCh38
NC_000023.10:g.153363076C= , CM000685.1:g.153363076C=	GRCh37
NC_000023.9:g.153016270C=	NCBI36
NG_007107.2:g.44503G=
NG_007107.3:g.44485G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700484.1:n.7G=
ENST00000303391.11:c.-114G= MANE Plus Clinical	ENSP00000301948.6:n.-114G=
ENST00000453960.7:c.47G= MANE Select	ENSP00000395535.2:p.Gly16=
ENST00000676382.1:n.7G=
ENST00000303391.10:c.-114G=	ENSP00000301948.6:n.-114G=
ENST00000369957.5:c.-114G=	ENSP00000358973.4:n.-114G=
ENST00000407218.5:c.47G=	ENSP00000384865.2:p.Gly16=
ENST00000453960.6:c.47G=	ENSP00000395535.2:p.Gly16=
ENST00000619732.4:c.-114G=	ENSP00000480973.1:n.-114G=
ENST00000627864.1:n.62G=
ENST00000628176.2:c.-114G=	ENSP00000486978.1:n.-114G=
ENST00000631210.1:n.305+7162G=
NM_001110792.1:c.47G=	NP_001104262.1:p.Gly16=
NM_001316337.1:c.-561G=	NP_001303266.1:n.-561G=
NM_004992.3:c.-114G=	NP_004983.1:n.-114G=
XM_005274682.3:c.-505G=	XP_005274739.1:n.-505G=
NM_001110792.2:c.47G= MANE Select	NP_001104262.1:p.Gly16=
NM_001316337.2:c.-561G=	NP_001303266.1:n.-561G=
NM_001369391.2:c.-856G=	NP_001356320.1:n.-856G=
NM_001369392.2:c.-505G=	NP_001356321.1:n.-505G=
NM_001369393.2:c.-381G=	NP_001356322.1:n.-381G=
NM_001386137.1:c.-786G=	NP_001373066.1:n.-786G=
NM_001386138.1:c.-674G=	NP_001373067.1:n.-674G=
NM_001386139.1:c.-550G=	NP_001373068.1:n.-550G=
NM_004992.4:c.-114G= MANE Plus Clinical	NP_004983.1:n.-114G=