Canonical Allele Identifier: CA415300983

Gene: MECP2

Linked Data

• gnomAD v4: X-154097611-C-A
• MyVariant Identifiers: chrX:g.153363068C>A (hg19) ; chrX:g.154097611C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097611C>A , CM000685.2:g.154097611C>A	GRCh38
NC_000023.10:g.153363068C>A , CM000685.1:g.153363068C>A	GRCh37
NC_000023.9:g.153016262C>A	NCBI36
NG_007107.2:g.44511G>T
NG_007107.3:g.44493G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700484.1:n.15G>T
ENST00000303391.11:c.-106G>T MANE Plus Clinical	ENSP00000301948.6:n.-106G>T
ENST00000453960.7:c.55G>T MANE Select	ENSP00000395535.2:p.Glu19Ter
ENST00000676382.1:n.15G>T
ENST00000303391.10:c.-106G>T	ENSP00000301948.6:n.-106G>T
ENST00000369957.5:c.-106G>T	ENSP00000358973.4:n.-106G>T
ENST00000407218.5:c.55G>T	ENSP00000384865.2:p.Glu19Ter
ENST00000453960.6:c.55G>T	ENSP00000395535.2:p.Glu19Ter
ENST00000619732.4:c.-106G>T	ENSP00000480973.1:n.-106G>T
ENST00000627864.1:n.70G>T
ENST00000628176.2:c.-106G>T	ENSP00000486978.1:n.-106G>T
ENST00000631210.1:n.305+7170G>T
NM_001110792.1:c.55G>T	NP_001104262.1:p.Glu19Ter
NM_001316337.1:c.-553G>T	NP_001303266.1:n.-553G>T
NM_004992.3:c.-106G>T	NP_004983.1:n.-106G>T
XM_005274682.3:c.-497G>T	XP_005274739.1:n.-497G>T
NM_001110792.2:c.55G>T MANE Select	NP_001104262.1:p.Glu19Ter
NM_001316337.2:c.-553G>T	NP_001303266.1:n.-553G>T
NM_001369391.2:c.-848G>T	NP_001356320.1:n.-848G>T
NM_001369392.2:c.-497G>T	NP_001356321.1:n.-497G>T
NM_001369393.2:c.-373G>T	NP_001356322.1:n.-373G>T
NM_001386137.1:c.-778G>T	NP_001373066.1:n.-778G>T
NM_001386138.1:c.-666G>T	NP_001373067.1:n.-666G>T
NM_001386139.1:c.-542G>T	NP_001373068.1:n.-542G>T
NM_004992.4:c.-106G>T MANE Plus Clinical	NP_004983.1:n.-106G>T