Canonical Allele Identifier: CA415299018

Gene: MECP2

Linked Data

• MyVariant Identifiers: chrX:g.153357654A>C (hg19) ; chrX:g.154092196A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154092196A>C , CM000685.2:g.154092196A>C	GRCh38
NC_000023.10:g.153357654A>C , CM000685.1:g.153357654A>C	GRCh37
NC_000023.9:g.153010848A>C	NCBI36
NG_007107.2:g.49925T>G
NG_007107.3:g.49908T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000700484.1:n.22+5408T>G
ENST00000303391.11:c.14T>G MANE Plus Clinical	ENSP00000301948.6:p.Met5Arg
ENST00000453960.7:c.62+5408T>G MANE Select	ENSP00000395535.2:n.62+5408T>G
ENST00000611468.2:n.112T>G
ENST00000630151.2:c.14T>G	ENSP00000486089.1:p.Met5Arg
ENST00000637533.1:n.57+4773T>G
ENST00000637791.1:n.66T>G
ENST00000674996.1:c.14T>G	ENSP00000502832.1:p.Met5Arg
ENST00000675526.1:c.14T>G	ENSP00000501710.1:p.Met5Arg
ENST00000675841.1:n.112T>G
ENST00000676382.1:n.22+5408T>G
ENST00000303391.10:c.14T>G	ENSP00000301948.6:p.Met5Arg
ENST00000369957.5:c.14T>G	ENSP00000358973.4:p.Met5Arg
ENST00000407218.5:c.62+5408T>G	ENSP00000384865.2:n.62+5408T>G
ENST00000415944.3:c.14T>G	ENSP00000416267.1:p.Met5Arg
ENST00000453960.6:c.62+5408T>G	ENSP00000395535.2:n.62+5408T>G
ENST00000496908.5:n.157+4617T>G
ENST00000611468.1:c.2T>G	ENSP00000479736.1:p.Met1Arg
ENST00000619732.4:c.14T>G	ENSP00000480973.1:p.Met5Arg
ENST00000622433.4:c.2T>G	ENSP00000484470.1:p.Met1Arg
ENST00000627864.1:n.189T>G
ENST00000628176.2:c.14T>G	ENSP00000486978.1:p.Met5Arg
ENST00000630151.1:c.14T>G	ENSP00000486089.1:p.Met5Arg
ENST00000631210.1:n.305+12585T>G
NM_001110792.1:c.62+5408T>G	NP_001104262.1:n.62+5408T>G
NM_001316337.1:c.-434T>G	NP_001303266.1:n.-434T>G
NM_004992.3:c.14T>G	NP_004983.1:p.Met5Arg
XM_005274681.3:c.14T>G	XP_005274738.1:p.Met5Arg
XM_005274682.3:c.-378T>G	XP_005274739.1:n.-378T>G
XM_024452383.1:c.-804T>G	XP_024308151.1:n.-804T>G
XM_024452384.1:c.-378T>G	XP_024308152.1:n.-378T>G
NM_001110792.2:c.62+5408T>G MANE Select	NP_001104262.1:n.62+5408T>G
NM_001316337.2:c.-434T>G	NP_001303266.1:n.-434T>G
NM_001369391.2:c.-729T>G	NP_001356320.1:n.-729T>G
NM_001369392.2:c.-378T>G	NP_001356321.1:n.-378T>G
NM_001369393.2:c.-366+5408T>G	NP_001356322.1:n.-366+5408T>G
NM_001369394.1:c.-254+4617T>G	NP_001356323.1:n.-254+4617T>G
NM_001369394.2:c.-254+4617T>G	NP_001356323.1:n.-254+4617T>G
NM_001386137.1:c.-659T>G	NP_001373066.1:n.-659T>G
NM_001386138.1:c.-547T>G	NP_001373067.1:n.-547T>G
NM_001386139.1:c.-535+5408T>G	NP_001373068.1:n.-535+5408T>G
NM_004992.4:c.14T>G MANE Plus Clinical	NP_004983.1:p.Met5Arg