Canonical Allele Identifier: CA873304040

Gene: MECP2

Linked Data

• dbSNP Id: rs1371620283
• gnomAD v3: X-154092002-C-CT
• gnomAD v4: X-154092002-C-CT
• MyVariant Identifiers: chrX:g.154092002_154092003insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154092010dup , CM000685.2:g.154092010dup	GRCh38
NC_000023.10:g.153357468dup , CM000685.1:g.153357468dup	GRCh37
NC_000023.9:g.153010662dup	NCBI36
NG_007107.2:g.50118dup
NG_007107.3:g.50101dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700484.1:n.22+5601dup
ENST00000303391.11:c.26+181dup MANE Plus Clinical	ENSP00000301948.6:n.26+181dup
ENST00000453960.7:c.62+5601dup MANE Select	ENSP00000395535.2:n.62+5601dup
ENST00000611468.2:n.124+181dup
ENST00000630151.2:c.26+181dup	ENSP00000486089.1:n.26+181dup
ENST00000637533.1:n.57+4966dup
ENST00000637791.1:n.78+181dup
ENST00000674996.1:c.26+181dup	ENSP00000502832.1:n.26+181dup
ENST00000675526.1:c.26+181dup	ENSP00000501710.1:n.26+181dup
ENST00000675841.1:n.124+181dup
ENST00000676382.1:n.22+5601dup
ENST00000303391.10:c.26+181dup	ENSP00000301948.6:n.26+181dup
ENST00000369957.5:c.26+181dup	ENSP00000358973.4:n.26+181dup
ENST00000407218.5:c.62+5601dup	ENSP00000384865.2:n.62+5601dup
ENST00000415944.3:c.26+181dup	ENSP00000416267.1:n.26+181dup
ENST00000453960.6:c.62+5601dup	ENSP00000395535.2:n.62+5601dup
ENST00000496908.5:n.157+4810dup
ENST00000611468.1:c.14+181dup	ENSP00000479736.1:n.14+181dup
ENST00000619732.4:c.26+181dup	ENSP00000480973.1:n.26+181dup
ENST00000622433.4:c.14+181dup	ENSP00000484470.1:n.14+181dup
ENST00000627864.1:n.201+181dup
ENST00000628176.2:c.26+181dup	ENSP00000486978.1:n.26+181dup
ENST00000630151.1:c.26+181dup	ENSP00000486089.1:n.26+181dup
ENST00000631210.1:n.305+12778dup
NM_001110792.1:c.62+5601dup	NP_001104262.1:n.62+5601dup
NM_001316337.1:c.-422+181dup	NP_001303266.1:n.-422+181dup
NM_004992.3:c.26+181dup	NP_004983.1:n.26+181dup
XM_005274681.3:c.26+181dup	XP_005274738.1:n.26+181dup
XM_005274682.3:c.-366+181dup	XP_005274739.1:n.-366+181dup
XM_024452383.1:c.-792+181dup	XP_024308151.1:n.-792+181dup
XM_024452384.1:c.-366+181dup	XP_024308152.1:n.-366+181dup
NM_001110792.2:c.62+5601dup MANE Select	NP_001104262.1:n.62+5601dup
NM_001316337.2:c.-422+181dup	NP_001303266.1:n.-422+181dup
NM_001369391.2:c.-717+181dup	NP_001356320.1:n.-717+181dup
NM_001369392.2:c.-366+181dup	NP_001356321.1:n.-366+181dup
NM_001369393.2:c.-366+5601dup	NP_001356322.1:n.-366+5601dup
NM_001369394.1:c.-254+4810dup	NP_001356323.1:n.-254+4810dup
NM_001369394.2:c.-254+4810dup	NP_001356323.1:n.-254+4810dup
NM_001386137.1:c.-647+181dup	NP_001373066.1:n.-647+181dup
NM_001386138.1:c.-535+181dup	NP_001373067.1:n.-535+181dup
NM_001386139.1:c.-535+5601dup	NP_001373068.1:n.-535+5601dup
NM_004992.4:c.26+181dup MANE Plus Clinical	NP_004983.1:n.26+181dup