Canonical Allele Identifier: CA2466594808

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097665T= , CM000685.2:g.154097665T=	GRCh38
NC_000023.10:g.153363122T= , CM000685.1:g.153363122T=	GRCh37
NC_000023.9:g.153016316T=	NCBI36
NG_007107.2:g.44457A=
NG_007107.3:g.44439A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000303391.11:c.-160A= MANE Plus Clinical	ENSP00000301948.6:n.-160A=
ENST00000453960.7:c.1A= MANE Select	ENSP00000395535.2:p.Met1=
ENST00000303391.10:c.-160A=	ENSP00000301948.6:n.-160A=
ENST00000407218.5:c.1A=	ENSP00000384865.2:p.Met1=
ENST00000453960.6:c.1A=	ENSP00000395535.2:p.Met1=
ENST00000619732.4:c.-160A=	ENSP00000480973.1:n.-160A=
ENST00000627864.1:n.16A=
ENST00000628176.2:c.-160A=	ENSP00000486978.1:n.-160A=
ENST00000631210.1:n.305+7116A=
NM_001110792.1:c.1A=	NP_001104262.1:p.Met1=
NM_001316337.1:c.-607A=	NP_001303266.1:n.-607A=
NM_004992.3:c.-160A=	NP_004983.1:n.-160A=
XM_005274682.3:c.-551A=	XP_005274739.1:n.-551A=
NM_001110792.2:c.1A= MANE Select	NP_001104262.1:p.Met1=
NM_001316337.2:c.-607A=	NP_001303266.1:n.-607A=
NM_001369391.2:c.-902A=	NP_001356320.1:n.-902A=
NM_001369392.2:c.-551A=	NP_001356321.1:n.-551A=
NM_001369393.2:c.-427A=	NP_001356322.1:n.-427A=
NM_001386137.1:c.-832A=	NP_001373066.1:n.-832A=
NM_001386138.1:c.-720A=	NP_001373067.1:n.-720A=
NM_001386139.1:c.-596A=	NP_001373068.1:n.-596A=
NM_004992.4:c.-160A= MANE Plus Clinical	NP_004983.1:n.-160A=