Canonical Allele Identifier: CA2466594758

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097608T= , CM000685.2:g.154097608T=	GRCh38
NC_000023.10:g.153363065T= , CM000685.1:g.153363065T=	GRCh37
NC_000023.9:g.153016259T=	NCBI36
NG_007107.2:g.44514A=
NG_007107.3:g.44496A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700484.1:n.18A=
ENST00000303391.11:c.-103A= MANE Plus Clinical	ENSP00000301948.6:n.-103A=
ENST00000453960.7:c.58A= MANE Select	ENSP00000395535.2:p.Arg20=
ENST00000676382.1:n.18A=
ENST00000303391.10:c.-103A=	ENSP00000301948.6:n.-103A=
ENST00000369957.5:c.-103A=	ENSP00000358973.4:n.-103A=
ENST00000407218.5:c.58A=	ENSP00000384865.2:p.Arg20=
ENST00000453960.6:c.58A=	ENSP00000395535.2:p.Arg20=
ENST00000619732.4:c.-103A=	ENSP00000480973.1:n.-103A=
ENST00000627864.1:n.73A=
ENST00000628176.2:c.-103A=	ENSP00000486978.1:n.-103A=
ENST00000631210.1:n.305+7173A=
NM_001110792.1:c.58A=	NP_001104262.1:p.Arg20=
NM_001316337.1:c.-550A=	NP_001303266.1:n.-550A=
NM_004992.3:c.-103A=	NP_004983.1:n.-103A=
XM_005274682.3:c.-494A=	XP_005274739.1:n.-494A=
NM_001110792.2:c.58A= MANE Select	NP_001104262.1:p.Arg20=
NM_001316337.2:c.-550A=	NP_001303266.1:n.-550A=
NM_001369391.2:c.-845A=	NP_001356320.1:n.-845A=
NM_001369392.2:c.-494A=	NP_001356321.1:n.-494A=
NM_001369393.2:c.-370A=	NP_001356322.1:n.-370A=
NM_001386137.1:c.-775A=	NP_001373066.1:n.-775A=
NM_001386138.1:c.-663A=	NP_001373067.1:n.-663A=
NM_001386139.1:c.-539A=	NP_001373068.1:n.-539A=
NM_004992.4:c.-103A= MANE Plus Clinical	NP_004983.1:n.-103A=