Canonical Allele Identifier: CA2466594821

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097690C= , CM000685.2:g.154097690C=	GRCh38
NC_000023.10:g.153363147C= , CM000685.1:g.153363147C=	GRCh37
NC_000023.9:g.153016341C=	NCBI36
NG_007107.2:g.44432G=
NG_007107.3:g.44414G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303391.11:c.-185G= MANE Plus Clinical	ENSP00000301948.6:n.-185G=
ENST00000453960.7:c.-25G= MANE Select	ENSP00000395535.2:n.-25G=
ENST00000303391.10:c.-185G=	ENSP00000301948.6:n.-185G=
ENST00000453960.6:c.-25G=	ENSP00000395535.2:n.-25G=
ENST00000619732.4:c.-185G=	ENSP00000480973.1:n.-185G=
ENST00000628176.2:c.-185G=	ENSP00000486978.1:n.-185G=
ENST00000631210.1:n.305+7091G=
NM_001110792.1:c.-25G=	NP_001104262.1:n.-25G=
NM_001316337.1:c.-632G=	NP_001303266.1:n.-632G=
NM_004992.3:c.-185G=	NP_004983.1:n.-185G=
NM_001110792.2:c.-25G= MANE Select	NP_001104262.1:n.-25G=
NM_001316337.2:c.-632G=	NP_001303266.1:n.-632G=
NM_001369391.2:c.-927G=	NP_001356320.1:n.-927G=
NM_001369392.2:c.-576G=	NP_001356321.1:n.-576G=
NM_001369393.2:c.-452G=	NP_001356322.1:n.-452G=
NM_001386137.1:c.-857G=	NP_001373066.1:n.-857G=
NM_001386138.1:c.-745G=	NP_001373067.1:n.-745G=
NM_001386139.1:c.-621G=	NP_001373068.1:n.-621G=
NM_004992.4:c.-185G= MANE Plus Clinical	NP_004983.1:n.-185G=