Canonical Allele Identifier: CA232871

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154030814G>A , CM000685.2:g.154030814G>A	GRCh38
NC_000023.10:g.153296265G>A , CM000685.1:g.153296265G>A	GRCh37
NC_000023.9:g.152949459G>A	NCBI36
NG_007107.2:g.111314C>T
NG_007107.3:g.111290C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001110792.2:c.1050C>T MANE Select	NP_001104262.1:p.Thr350=
ENST00000453960.7:c.1050C>T MANE Select	ENSP00000395535.2:p.Thr350=
NM_004992.4:c.1014C>T MANE Plus Clinical	NP_004983.1:p.Thr338=
ENST00000303391.11:c.1014C>T MANE Plus Clinical	ENSP00000301948.6:p.Thr338=
NM_001110792.1:c.1050C>T	NP_001104262.1:p.Thr350=
NM_001316337.1:c.735C>T	NP_001303266.1:p.Thr245=
NM_001316337.2:c.735C>T	NP_001303266.1:p.Thr245=
NM_001369391.2:c.735C>T	NP_001356320.1:p.Thr245=
NM_001369392.2:c.735C>T	NP_001356321.1:p.Thr245=
NM_001369393.2:c.735C>T	NP_001356322.1:p.Thr245=
NM_001369394.1:c.735C>T	NP_001356323.1:p.Thr245=
NM_001369394.2:c.735C>T	NP_001356323.1:p.Thr245=
NM_001386137.1:c.345C>T	NP_001373066.1:p.Thr115=
NM_001386138.1:c.345C>T	NP_001373067.1:p.Thr115=
NM_001386139.1:c.345C>T	NP_001373068.1:p.Thr115=
NM_004992.3:c.1014C>T	NP_004983.1:p.Thr338=
ENST00000303391.10:c.1014C>T	ENSP00000301948.6:p.Thr338=
ENST00000407218.5:c.*386C>T	ENSP00000384865.2:n.*386C>T
ENST00000453960.6:c.1050C>T	ENSP00000395535.2:p.Thr350=
ENST00000619732.4:c.1014C>T	ENSP00000480973.1:p.Thr338=
ENST00000628176.2:c.*386C>T	ENSP00000486978.1:n.*386C>T
XM_005274681.3:c.1014C>T	XP_005274738.1:p.Thr338=
XM_005274682.3:c.735C>T	XP_005274739.1:p.Thr245=
XM_005274683.3:c.735C>T	XP_005274740.1:p.Thr245=
XM_006724819.2:c.345C>T	XP_006724882.1:p.Thr115=
XM_006724819.3:c.345C>T	XP_006724882.1:p.Thr115=
XM_011531166.1:c.735C>T	XP_011529468.1:p.Thr245=
XM_011531166.2:c.735C>T	XP_011529468.1:p.Thr245=
XM_024452383.1:c.735C>T	XP_024308151.1:p.Thr245=
XM_024452384.1:c.735C>T	XP_024308152.1:p.Thr245=