Canonical Allele Identifier: CA2466568119

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154026640C= , CM000685.2:g.154026640C=	GRCh38
NC_000023.10:g.153292091C= , CM000685.1:g.153292091C=	GRCh37
NC_000023.9:g.152945285C=	NCBI36
NG_007107.2:g.115488G=
NG_007107.3:g.115464G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303391.11:c.*3727G= MANE Plus Clinical	ENSP00000301948.6:n.*3727G=
ENST00000453960.7:c.*3727G= MANE Select	ENSP00000395535.2:n.*3727G=
ENST00000303391.10:c.*3727G=	ENSP00000301948.6:n.*3727G=
ENST00000619732.4:c.*3654G=	ENSP00000480973.1:n.*3654G=
NM_004992.3:c.*3727G=	NP_004983.1:n.*3727G=
XM_006724819.3:c.*3727G=	XP_006724882.1:n.*3727G=
XM_011531166.2:c.*3727G=	XP_011529468.1:n.*3727G=
XM_024452383.1:c.*3727G=	XP_024308151.1:n.*3727G=
XM_024452384.1:c.*3727G=	XP_024308152.1:n.*3727G=
NM_001110792.2:c.*3727G= MANE Select	NP_001104262.1:n.*3727G=
NM_001316337.2:c.*3727G=	NP_001303266.1:n.*3727G=
NM_001369391.2:c.*3727G=	NP_001356320.1:n.*3727G=
NM_001369392.2:c.*3727G=	NP_001356321.1:n.*3727G=
NM_001369393.2:c.*3727G=	NP_001356322.1:n.*3727G=
NM_001369394.2:c.*3727G=	NP_001356323.1:n.*3727G=
NM_001386137.1:c.*3727G=	NP_001373066.1:n.*3727G=
NM_001386138.1:c.*3727G=	NP_001373067.1:n.*3727G=
NM_001386139.1:c.*3727G=	NP_001373068.1:n.*3727G=
NM_004992.4:c.*3727G= MANE Plus Clinical	NP_004983.1:n.*3727G=