Canonical Allele Identifier: CA2466594778

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097632C= , CM000685.2:g.154097632C=	GRCh38
NC_000023.10:g.153363089C= , CM000685.1:g.153363089C=	GRCh37
NC_000023.9:g.153016283C=	NCBI36
NG_007107.2:g.44490G=
NG_007107.3:g.44472G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303391.11:c.-127G= MANE Plus Clinical	ENSP00000301948.6:n.-127G=
ENST00000453960.7:c.34G= MANE Select	ENSP00000395535.2:p.Gly12=
ENST00000303391.10:c.-127G=	ENSP00000301948.6:n.-127G=
ENST00000369957.5:c.-127G=	ENSP00000358973.4:n.-127G=
ENST00000407218.5:c.34G=	ENSP00000384865.2:p.Gly12=
ENST00000453960.6:c.34G=	ENSP00000395535.2:p.Gly12=
ENST00000619732.4:c.-127G=	ENSP00000480973.1:n.-127G=
ENST00000627864.1:n.49G=
ENST00000628176.2:c.-127G=	ENSP00000486978.1:n.-127G=
ENST00000631210.1:n.305+7149G=
NM_001110792.1:c.34G=	NP_001104262.1:p.Gly12=
NM_001316337.1:c.-574G=	NP_001303266.1:n.-574G=
NM_004992.3:c.-127G=	NP_004983.1:n.-127G=
XM_005274682.3:c.-518G=	XP_005274739.1:n.-518G=
NM_001110792.2:c.34G= MANE Select	NP_001104262.1:p.Gly12=
NM_001316337.2:c.-574G=	NP_001303266.1:n.-574G=
NM_001369391.2:c.-869G=	NP_001356320.1:n.-869G=
NM_001369392.2:c.-518G=	NP_001356321.1:n.-518G=
NM_001369393.2:c.-394G=	NP_001356322.1:n.-394G=
NM_001386137.1:c.-799G=	NP_001373066.1:n.-799G=
NM_001386138.1:c.-687G=	NP_001373067.1:n.-687G=
NM_001386139.1:c.-563G=	NP_001373068.1:n.-563G=
NM_004992.4:c.-127G= MANE Plus Clinical	NP_004983.1:n.-127G=