Canonical Allele Identifier: CA2466594809

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097671G= , CM000685.2:g.154097671G=	GRCh38
NC_000023.10:g.153363128G= , CM000685.1:g.153363128G=	GRCh37
NC_000023.9:g.153016322G=	NCBI36
NG_007107.2:g.44451C=
NG_007107.3:g.44433C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000303391.11:c.-166C= MANE Plus Clinical	ENSP00000301948.6:n.-166C=
ENST00000453960.7:c.-6C= MANE Select	ENSP00000395535.2:n.-6C=
ENST00000303391.10:c.-166C=	ENSP00000301948.6:n.-166C=
ENST00000407218.5:c.-6C=	ENSP00000384865.2:n.-6C=
ENST00000453960.6:c.-6C=	ENSP00000395535.2:n.-6C=
ENST00000619732.4:c.-166C=	ENSP00000480973.1:n.-166C=
ENST00000627864.1:n.10C=
ENST00000628176.2:c.-166C=	ENSP00000486978.1:n.-166C=
ENST00000631210.1:n.305+7110C=
NM_001110792.1:c.-6C=	NP_001104262.1:n.-6C=
NM_001316337.1:c.-613C=	NP_001303266.1:n.-613C=
NM_004992.3:c.-166C=	NP_004983.1:n.-166C=
XM_005274682.3:c.-557C=	XP_005274739.1:n.-557C=
NM_001110792.2:c.-6C= MANE Select	NP_001104262.1:n.-6C=
NM_001316337.2:c.-613C=	NP_001303266.1:n.-613C=
NM_001369391.2:c.-908C=	NP_001356320.1:n.-908C=
NM_001369392.2:c.-557C=	NP_001356321.1:n.-557C=
NM_001369393.2:c.-433C=	NP_001356322.1:n.-433C=
NM_001386137.1:c.-838C=	NP_001373066.1:n.-838C=
NM_001386138.1:c.-726C=	NP_001373067.1:n.-726C=
NM_001386139.1:c.-602C=	NP_001373068.1:n.-602C=
NM_004992.4:c.-166C= MANE Plus Clinical	NP_004983.1:n.-166C=