Canonical Allele Identifier: CA915952025

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154030700_154032236del , CM000685.2:g.154030700_154032236del	GRCh38
NC_000023.10:g.153296151_153297687del , CM000685.1:g.153296151_153297687del	GRCh37
NC_000023.9:g.152949345_152950881del	NCBI36
NG_007107.2:g.109892_111428del
NG_007107.3:g.109868_111404del

Transcript Alleles

HGVS	Amino-acid change
ENST00000303391.11:c.348_1128del
ENST00000453960.7:c.384_1164del
ENST00000303391.10:c.348_1128del
ENST00000407218.5:c.384_*500del
ENST00000453960.6:c.384_1164del
ENST00000619732.4:c.348_1128del
ENST00000628176.2:c.348_*500del
NM_001110792.1:c.384_1164del
NM_001316337.1:c.69_849del
NM_004992.3:c.348_1128del
XM_005274681.3:c.348_1128del
XM_005274682.3:c.69_849del
XM_005274683.3:c.69_849del
XM_011531166.1:c.69_849del
XM_006724819.3:c.-213_459del
XM_011531166.2:c.69_849del
XM_024452383.1:c.69_849del
XM_024452384.1:c.69_849del
NM_001110792.2:c.384_1164del
NM_001316337.2:c.69_849del
NM_001369391.2:c.69_849del
NM_001369392.2:c.69_849del
NM_001369393.2:c.69_849del
NM_001369394.1:c.69_849del
NM_001369394.2:c.69_849del
NM_001386137.1:c.-213_459del
NM_001386138.1:c.-213_459del
NM_001386139.1:c.-213_459del
NM_004992.4:c.348_1128del