Canonical Allele Identifier: CA2695105338

Gene: MECP2

Linked Data

• gnomAD v4: X-154097552-CCCCCGCCCCCCGGCAAGGGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097561_154097580del , CM000685.2:g.154097561_154097580del	GRCh38
NC_000023.10:g.153363018_153363037del , CM000685.1:g.153363018_153363037del	GRCh37
NC_000023.9:g.153016212_153016231del	NCBI36
NG_007107.2:g.44550_44569del
NG_007107.3:g.44532_44551del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700484.1:n.22+32_22+51del
ENST00000303391.11:c.-99+32_-99+51del MANE Plus Clinical	ENSP00000301948.6:n.-99+32_-99+51del
ENST00000453960.7:c.62+32_62+51del MANE Select	ENSP00000395535.2:n.62+32_62+51del
ENST00000676382.1:n.22+32_22+51del
ENST00000303391.10:c.-99+32_-99+51del	ENSP00000301948.6:n.-99+32_-99+51del
ENST00000369957.5:c.-99+32_-99+51del	ENSP00000358973.4:n.-99+32_-99+51del
ENST00000407218.5:c.62+32_62+51del	ENSP00000384865.2:n.62+32_62+51del
ENST00000453960.6:c.62+32_62+51del	ENSP00000395535.2:n.62+32_62+51del
ENST00000619732.4:c.-99+32_-99+51del	ENSP00000480973.1:n.-99+32_-99+51del
ENST00000627864.1:n.77+32_77+51del
ENST00000628176.2:c.-99+32_-99+51del	ENSP00000486978.1:n.-99+32_-99+51del
ENST00000631210.1:n.305+7209_305+7228del
NM_001110792.1:c.62+32_62+51del	NP_001104262.1:n.62+32_62+51del
NM_001316337.1:c.-546+32_-546+51del	NP_001303266.1:n.-546+32_-546+51del
NM_004992.3:c.-99+32_-99+51del	NP_004983.1:n.-99+32_-99+51del
XM_005274682.3:c.-490+32_-490+51del	XP_005274739.1:n.-490+32_-490+51del
NM_001110792.2:c.62+32_62+51del MANE Select	NP_001104262.1:n.62+32_62+51del
NM_001316337.2:c.-546+32_-546+51del	NP_001303266.1:n.-546+32_-546+51del
NM_001369391.2:c.-841+32_-841+51del	NP_001356320.1:n.-841+32_-841+51del
NM_001369392.2:c.-490+32_-490+51del	NP_001356321.1:n.-490+32_-490+51del
NM_001369393.2:c.-366+32_-366+51del	NP_001356322.1:n.-366+32_-366+51del
NM_001386137.1:c.-771+32_-771+51del	NP_001373066.1:n.-771+32_-771+51del
NM_001386138.1:c.-659+32_-659+51del	NP_001373067.1:n.-659+32_-659+51del
NM_001386139.1:c.-535+32_-535+51del	NP_001373068.1:n.-535+32_-535+51del
NM_004992.4:c.-99+32_-99+51del MANE Plus Clinical	NP_004983.1:n.-99+32_-99+51del