Canonical Allele Identifier: CA2466570900

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154031225C= , CM000685.2:g.154031225C=	GRCh38
NC_000023.10:g.153296676C= , CM000685.1:g.153296676C=	GRCh37
NC_000023.9:g.152949870C=	NCBI36
NG_007107.2:g.110903G=
NG_007107.3:g.110879G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303391.11:c.603G= MANE Plus Clinical	ENSP00000301948.6:p.Ala201=
ENST00000453960.7:c.639G= MANE Select	ENSP00000395535.2:p.Ala213=
ENST00000637917.1:c.65+171G=
ENST00000303391.10:c.603G=	ENSP00000301948.6:p.Ala201=
ENST00000407218.5:c.530G=	ENSP00000384865.2:p.Arg177=
ENST00000453960.6:c.639G=	ENSP00000395535.2:p.Ala213=
ENST00000619732.4:c.603G=	ENSP00000480973.1:p.Ala201=
ENST00000622433.4:c.591G=	ENSP00000484470.1:p.Ala197=
ENST00000628176.2:c.494G=	ENSP00000486978.1:p.Arg165=
NM_001110792.1:c.639G=	NP_001104262.1:p.Ala213=
NM_001316337.1:c.324G=	NP_001303266.1:p.Ala108=
NM_004992.3:c.603G=	NP_004983.1:p.Ala201=
XM_005274681.3:c.603G=	XP_005274738.1:p.Ala201=
XM_005274682.3:c.324G=	XP_005274739.1:p.Ala108=
XM_005274683.3:c.324G=	XP_005274740.1:p.Ala108=
XM_006724819.2:c.-67G=	XP_006724882.1:n.-67G=
XM_011531166.1:c.324G=	XP_011529468.1:p.Ala108=
XM_006724819.3:c.-67G=	XP_006724882.1:n.-67G=
XM_011531166.2:c.324G=	XP_011529468.1:p.Ala108=
XM_024452383.1:c.324G=	XP_024308151.1:p.Ala108=
XM_024452384.1:c.324G=	XP_024308152.1:p.Ala108=
NM_001110792.2:c.639G= MANE Select	NP_001104262.1:p.Ala213=
NM_001316337.2:c.324G=	NP_001303266.1:p.Ala108=
NM_001369391.2:c.324G=	NP_001356320.1:p.Ala108=
NM_001369392.2:c.324G=	NP_001356321.1:p.Ala108=
NM_001369393.2:c.324G=	NP_001356322.1:p.Ala108=
NM_001369394.1:c.324G=	NP_001356323.1:p.Ala108=
NM_001369394.2:c.324G=	NP_001356323.1:p.Ala108=
NM_001386137.1:c.-67G=	NP_001373066.1:n.-67G=
NM_001386138.1:c.-67G=	NP_001373067.1:n.-67G=
NM_001386139.1:c.-67G=	NP_001373068.1:n.-67G=
NM_004992.4:c.603G= MANE Plus Clinical	NP_004983.1:p.Ala201=