Canonical Allele Identifier: CA2466570882

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154031206G= , CM000685.2:g.154031206G=	GRCh38
NC_000023.10:g.153296657G= , CM000685.1:g.153296657G=	GRCh37
NC_000023.9:g.152949851G=	NCBI36
NG_007107.2:g.110922C=
NG_007107.3:g.110898C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303391.11:c.622C= MANE Plus Clinical	ENSP00000301948.6:p.Gln208=
ENST00000453960.7:c.658C= MANE Select	ENSP00000395535.2:p.Gln220=
ENST00000637917.1:c.65+190C=
ENST00000303391.10:c.622C=	ENSP00000301948.6:p.Gln208=
ENST00000407218.5:c.549C=	ENSP00000384865.2:p.Cys183=
ENST00000453960.6:c.658C=	ENSP00000395535.2:p.Gln220=
ENST00000619732.4:c.622C=	ENSP00000480973.1:p.Gln208=
ENST00000622433.4:c.610C=	ENSP00000484470.1:p.Gln204=
ENST00000628176.2:c.513C=	ENSP00000486978.1:p.Cys171=
NM_001110792.1:c.658C=	NP_001104262.1:p.Gln220=
NM_001316337.1:c.343C=	NP_001303266.1:p.Gln115=
NM_004992.3:c.622C=	NP_004983.1:p.Gln208=
XM_005274681.3:c.622C=	XP_005274738.1:p.Gln208=
XM_005274682.3:c.343C=	XP_005274739.1:p.Gln115=
XM_005274683.3:c.343C=	XP_005274740.1:p.Gln115=
XM_006724819.2:c.-48C=	XP_006724882.1:n.-48C=
XM_011531166.1:c.343C=	XP_011529468.1:p.Gln115=
XM_006724819.3:c.-48C=	XP_006724882.1:n.-48C=
XM_011531166.2:c.343C=	XP_011529468.1:p.Gln115=
XM_024452383.1:c.343C=	XP_024308151.1:p.Gln115=
XM_024452384.1:c.343C=	XP_024308152.1:p.Gln115=
NM_001110792.2:c.658C= MANE Select	NP_001104262.1:p.Gln220=
NM_001316337.2:c.343C=	NP_001303266.1:p.Gln115=
NM_001369391.2:c.343C=	NP_001356320.1:p.Gln115=
NM_001369392.2:c.343C=	NP_001356321.1:p.Gln115=
NM_001369393.2:c.343C=	NP_001356322.1:p.Gln115=
NM_001369394.1:c.343C=	NP_001356323.1:p.Gln115=
NM_001369394.2:c.343C=	NP_001356323.1:p.Gln115=
NM_001386137.1:c.-48C=	NP_001373066.1:n.-48C=
NM_001386138.1:c.-48C=	NP_001373067.1:n.-48C=
NM_001386139.1:c.-48C=	NP_001373068.1:n.-48C=
NM_004992.4:c.622C= MANE Plus Clinical	NP_004983.1:p.Gln208=