Canonical Allele Identifier: CA2466570859

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154031174_154031187delinsCCCAGGACTTTTCT , CM000685.2:g.154031174_154031187delinsCCCAGGACTTTTCT	GRCh38
NC_000023.10:g.153296625_153296638delinsCCCAGGACTTTTCT , CM000685.1:g.153296625_153296638delinsCCCAGGACTTTTCT	GRCh37
NC_000023.9:g.152949819_152949832delinsCCCAGGACTTTTCT	NCBI36
NG_007107.2:g.110941_110954delinsAGAAAAGTCCTGGG
NG_007107.3:g.110917_110930delinsAGAAAAGTCCTGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000303391.11:c.641_654delinsAGAAAAGTCCTGGG MANE Plus Clinical	ENSP00000301948.6:p.Glu214=
ENST00000453960.7:c.677_690delinsAGAAAAGTCCTGGG MANE Select	ENSP00000395535.2:p.Glu226=
ENST00000637917.1:c.65+209_65+222delinsAGAAAAGTCCTGGG
ENST00000303391.10:c.641_654delinsAGAAAAGTCCTGGG	ENSP00000301948.6:p.Glu214=
ENST00000407218.5:c.*13_*26delinsAGAAAAGTCCTGGG	ENSP00000384865.2:n.*13_*26delinsAGAAAAGTCCTGGG
ENST00000453960.6:c.677_690delinsAGAAAAGTCCTGGG	ENSP00000395535.2:p.Glu226=
ENST00000619732.4:c.641_654delinsAGAAAAGTCCTGGG	ENSP00000480973.1:p.Glu214=
ENST00000622433.4:c.629_642delinsAGAAAAGTCCTGGG	ENSP00000484470.1:p.Glu210=
ENST00000628176.2:c.*13_*26delinsAGAAAAGTCCTGGG	ENSP00000486978.1:n.*13_*26delinsAGAAAAGTCCTGGG
NM_001110792.1:c.677_690delinsAGAAAAGTCCTGGG	NP_001104262.1:p.Glu226=
NM_001316337.1:c.362_375delinsAGAAAAGTCCTGGG	NP_001303266.1:p.Glu121=
NM_004992.3:c.641_654delinsAGAAAAGTCCTGGG	NP_004983.1:p.Glu214=
XM_005274681.3:c.641_654delinsAGAAAAGTCCTGGG	XP_005274738.1:p.Glu214=
XM_005274682.3:c.362_375delinsAGAAAAGTCCTGGG	XP_005274739.1:p.Glu121=
XM_005274683.3:c.362_375delinsAGAAAAGTCCTGGG	XP_005274740.1:p.Glu121=
XM_006724819.2:c.-29_-16delinsAGAAAAGTCCTGGG	XP_006724882.1:n.-29_-16delinsAGAAAAGTCCTGGG
XM_011531166.1:c.362_375delinsAGAAAAGTCCTGGG	XP_011529468.1:p.Glu121=
XM_006724819.3:c.-29_-16delinsAGAAAAGTCCTGGG	XP_006724882.1:n.-29_-16delinsAGAAAAGTCCTGGG
XM_011531166.2:c.362_375delinsAGAAAAGTCCTGGG	XP_011529468.1:p.Glu121=
XM_024452383.1:c.362_375delinsAGAAAAGTCCTGGG	XP_024308151.1:p.Glu121=
XM_024452384.1:c.362_375delinsAGAAAAGTCCTGGG	XP_024308152.1:p.Glu121=
NM_001110792.2:c.677_690delinsAGAAAAGTCCTGGG MANE Select	NP_001104262.1:p.Glu226=
NM_001316337.2:c.362_375delinsAGAAAAGTCCTGGG	NP_001303266.1:p.Glu121=
NM_001369391.2:c.362_375delinsAGAAAAGTCCTGGG	NP_001356320.1:p.Glu121=
NM_001369392.2:c.362_375delinsAGAAAAGTCCTGGG	NP_001356321.1:p.Glu121=
NM_001369393.2:c.362_375delinsAGAAAAGTCCTGGG	NP_001356322.1:p.Glu121=
NM_001369394.1:c.362_375delinsAGAAAAGTCCTGGG	NP_001356323.1:p.Glu121=
NM_001369394.2:c.362_375delinsAGAAAAGTCCTGGG	NP_001356323.1:p.Glu121=
NM_001386137.1:c.-29_-16delinsAGAAAAGTCCTGGG	NP_001373066.1:n.-29_-16delinsAGAAAAGTCCTGGG
NM_001386138.1:c.-29_-16delinsAGAAAAGTCCTGGG	NP_001373067.1:n.-29_-16delinsAGAAAAGTCCTGGG
NM_001386139.1:c.-29_-16delinsAGAAAAGTCCTGGG	NP_001373068.1:n.-29_-16delinsAGAAAAGTCCTGGG
NM_004992.4:c.641_654delinsAGAAAAGTCCTGGG MANE Plus Clinical	NP_004983.1:p.Glu214=