Canonical Allele Identifier: CA415301563

Gene: MECP2

Linked Data

• gnomAD v4: X-154097652-G-A
• MyVariant Identifiers: chrX:g.153363109G>A (hg19) ; chrX:g.154097652G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097652G>A , CM000685.2:g.154097652G>A	GRCh38
NC_000023.10:g.153363109G>A , CM000685.1:g.153363109G>A	GRCh37
NC_000023.9:g.153016303G>A	NCBI36
NG_007107.2:g.44470C>T
NG_007107.3:g.44452C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303391.11:c.-147C>T MANE Plus Clinical	ENSP00000301948.6:n.-147C>T
ENST00000453960.7:c.14C>T MANE Select	ENSP00000395535.2:p.Ala5Val
ENST00000303391.10:c.-147C>T	ENSP00000301948.6:n.-147C>T
ENST00000369957.5:c.-147C>T	ENSP00000358973.4:n.-147C>T
ENST00000407218.5:c.14C>T	ENSP00000384865.2:p.Ala5Val
ENST00000453960.6:c.14C>T	ENSP00000395535.2:p.Ala5Val
ENST00000619732.4:c.-147C>T	ENSP00000480973.1:n.-147C>T
ENST00000627864.1:n.29C>T
ENST00000628176.2:c.-147C>T	ENSP00000486978.1:n.-147C>T
ENST00000631210.1:n.305+7129C>T
NM_001110792.1:c.14C>T	NP_001104262.1:p.Ala5Val
NM_001316337.1:c.-594C>T	NP_001303266.1:n.-594C>T
NM_004992.3:c.-147C>T	NP_004983.1:n.-147C>T
XM_005274682.3:c.-538C>T	XP_005274739.1:n.-538C>T
NM_001110792.2:c.14C>T MANE Select	NP_001104262.1:p.Ala5Val
NM_001316337.2:c.-594C>T	NP_001303266.1:n.-594C>T
NM_001369391.2:c.-889C>T	NP_001356320.1:n.-889C>T
NM_001369392.2:c.-538C>T	NP_001356321.1:n.-538C>T
NM_001369393.2:c.-414C>T	NP_001356322.1:n.-414C>T
NM_001386137.1:c.-819C>T	NP_001373066.1:n.-819C>T
NM_001386138.1:c.-707C>T	NP_001373067.1:n.-707C>T
NM_001386139.1:c.-583C>T	NP_001373068.1:n.-583C>T
NM_004992.4:c.-147C>T MANE Plus Clinical	NP_004983.1:n.-147C>T