Canonical Allele Identifier: CA2466594799

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097656C= , CM000685.2:g.154097656C=	GRCh38
NC_000023.10:g.153363113C= , CM000685.1:g.153363113C=	GRCh37
NC_000023.9:g.153016307C=	NCBI36
NG_007107.2:g.44466G=
NG_007107.3:g.44448G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303391.11:c.-151G= MANE Plus Clinical	ENSP00000301948.6:n.-151G=
ENST00000453960.7:c.10G= MANE Select	ENSP00000395535.2:p.Ala4=
ENST00000303391.10:c.-151G=	ENSP00000301948.6:n.-151G=
ENST00000369957.5:c.-151G=	ENSP00000358973.4:n.-151G=
ENST00000407218.5:c.10G=	ENSP00000384865.2:p.Ala4=
ENST00000453960.6:c.10G=	ENSP00000395535.2:p.Ala4=
ENST00000619732.4:c.-151G=	ENSP00000480973.1:n.-151G=
ENST00000627864.1:n.25G=
ENST00000628176.2:c.-151G=	ENSP00000486978.1:n.-151G=
ENST00000631210.1:n.305+7125G=
NM_001110792.1:c.10G=	NP_001104262.1:p.Ala4=
NM_001316337.1:c.-598G=	NP_001303266.1:n.-598G=
NM_004992.3:c.-151G=	NP_004983.1:n.-151G=
XM_005274682.3:c.-542G=	XP_005274739.1:n.-542G=
NM_001110792.2:c.10G= MANE Select	NP_001104262.1:p.Ala4=
NM_001316337.2:c.-598G=	NP_001303266.1:n.-598G=
NM_001369391.2:c.-893G=	NP_001356320.1:n.-893G=
NM_001369392.2:c.-542G=	NP_001356321.1:n.-542G=
NM_001369393.2:c.-418G=	NP_001356322.1:n.-418G=
NM_001386137.1:c.-823G=	NP_001373066.1:n.-823G=
NM_001386138.1:c.-711G=	NP_001373067.1:n.-711G=
NM_001386139.1:c.-587G=	NP_001373068.1:n.-587G=
NM_004992.4:c.-151G= MANE Plus Clinical	NP_004983.1:n.-151G=