Canonical Allele Identifier: CA2695105458

Gene: MECP2

Linked Data

• gnomAD v4: X-154097670-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097670C>T , CM000685.2:g.154097670C>T	GRCh38
NC_000023.10:g.153363127C>T , CM000685.1:g.153363127C>T	GRCh37
NC_000023.9:g.153016321C>T	NCBI36
NG_007107.2:g.44452G>A
NG_007107.3:g.44434G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000303391.11:c.-165G>A MANE Plus Clinical	ENSP00000301948.6:n.-165G>A
ENST00000453960.7:c.-5G>A MANE Select	ENSP00000395535.2:n.-5G>A
ENST00000303391.10:c.-165G>A	ENSP00000301948.6:n.-165G>A
ENST00000407218.5:c.-5G>A	ENSP00000384865.2:n.-5G>A
ENST00000453960.6:c.-5G>A	ENSP00000395535.2:n.-5G>A
ENST00000619732.4:c.-165G>A	ENSP00000480973.1:n.-165G>A
ENST00000627864.1:n.11G>A
ENST00000628176.2:c.-165G>A	ENSP00000486978.1:n.-165G>A
ENST00000631210.1:n.305+7111G>A
NM_001110792.1:c.-5G>A	NP_001104262.1:n.-5G>A
NM_001316337.1:c.-612G>A	NP_001303266.1:n.-612G>A
NM_004992.3:c.-165G>A	NP_004983.1:n.-165G>A
XM_005274682.3:c.-556G>A	XP_005274739.1:n.-556G>A
NM_001110792.2:c.-5G>A MANE Select	NP_001104262.1:n.-5G>A
NM_001316337.2:c.-612G>A	NP_001303266.1:n.-612G>A
NM_001369391.2:c.-907G>A	NP_001356320.1:n.-907G>A
NM_001369392.2:c.-556G>A	NP_001356321.1:n.-556G>A
NM_001369393.2:c.-432G>A	NP_001356322.1:n.-432G>A
NM_001386137.1:c.-837G>A	NP_001373066.1:n.-837G>A
NM_001386138.1:c.-725G>A	NP_001373067.1:n.-725G>A
NM_001386139.1:c.-601G>A	NP_001373068.1:n.-601G>A
NM_004992.4:c.-165G>A MANE Plus Clinical	NP_004983.1:n.-165G>A