Canonical Allele Identifier: CA2466571551

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154032287G= , CM000685.2:g.154032287G=	GRCh38
NC_000023.10:g.153297738G= , CM000685.1:g.153297738G=	GRCh37
NC_000023.9:g.152950932G=	NCBI36
NG_007107.2:g.109841C=
NG_007107.3:g.109817C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000303391.11:c.297C= MANE Plus Clinical	ENSP00000301948.6:p.Thr99=
ENST00000453960.7:c.333C= MANE Select	ENSP00000395535.2:p.Thr111=
ENST00000303391.10:c.297C=	ENSP00000301948.6:p.Thr99=
ENST00000369957.5:c.*351C=	ENSP00000358973.4:n.*351C=
ENST00000407218.5:c.333C=	ENSP00000384865.2:p.Thr111=
ENST00000453960.6:c.333C=	ENSP00000395535.2:p.Thr111=
ENST00000486506.5:n.2645C=
ENST00000611468.1:c.285C=	ENSP00000479736.1:p.Thr95=
ENST00000619732.4:c.297C=	ENSP00000480973.1:p.Thr99=
ENST00000622433.4:c.285C=	ENSP00000484470.1:p.Thr95=
ENST00000628176.2:c.297C=	ENSP00000486978.1:p.Thr99=
NM_001110792.1:c.333C=	NP_001104262.1:p.Thr111=
NM_001316337.1:c.18C=	NP_001303266.1:p.Thr6=
NM_004992.3:c.297C=	NP_004983.1:p.Thr99=
XM_005274681.3:c.297C=	XP_005274738.1:p.Thr99=
XM_005274682.3:c.18C=	XP_005274739.1:p.Thr6=
XM_005274683.3:c.18C=	XP_005274740.1:p.Thr6=
XM_011531166.1:c.18C=	XP_011529468.1:p.Thr6=
XM_006724819.3:c.-264C=	XP_006724882.1:n.-264C=
XM_011531166.2:c.18C=	XP_011529468.1:p.Thr6=
XM_024452383.1:c.18C=	XP_024308151.1:p.Thr6=
XM_024452384.1:c.18C=	XP_024308152.1:p.Thr6=
NM_001110792.2:c.333C= MANE Select	NP_001104262.1:p.Thr111=
NM_001316337.2:c.18C=	NP_001303266.1:p.Thr6=
NM_001369391.2:c.18C=	NP_001356320.1:p.Thr6=
NM_001369392.2:c.18C=	NP_001356321.1:p.Thr6=
NM_001369393.2:c.18C=	NP_001356322.1:p.Thr6=
NM_001369394.1:c.18C=	NP_001356323.1:p.Thr6=
NM_001369394.2:c.18C=	NP_001356323.1:p.Thr6=
NM_001386137.1:c.-264C=	NP_001373066.1:n.-264C=
NM_001386138.1:c.-264C=	NP_001373067.1:n.-264C=
NM_001386139.1:c.-264C=	NP_001373068.1:n.-264C=
NM_004992.4:c.297C= MANE Plus Clinical	NP_004983.1:p.Thr99=