Canonical Allele Identifier: CA2695202122

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154030546_154032241del , CM000685.2:g.154030546_154032241del	GRCh38
NC_000023.10:g.153295997_153297692del , CM000685.1:g.153295997_153297692del	GRCh37
NC_000023.9:g.152949191_152950886del	NCBI36
NG_007107.2:g.109887_111582del
NG_007107.3:g.109863_111558del

Transcript Alleles

HGVS	Amino-acid change
ENST00000303391.11:c.343_1282del
ENST00000453960.7:c.379_1318del
ENST00000303391.10:c.343_1282del
ENST00000453960.6:c.379_1318del
ENST00000619732.4:c.343_1282del
ENST00000628176.2:c.343_*654del
NM_001110792.1:c.379_1318del
NM_001316337.1:c.64_1003del
NM_004992.3:c.343_1282del
XM_005274681.3:c.343_1282del
XM_005274682.3:c.64_1003del
XM_005274683.3:c.64_1003del
XM_011531166.1:c.64_1003del
XM_006724819.3:c.-218_613del
XM_011531166.2:c.64_1003del
XM_024452383.1:c.64_1003del
XM_024452384.1:c.64_1003del
NM_001110792.2:c.379_1318del
NM_001316337.2:c.64_1003del
NM_001369391.2:c.64_1003del
NM_001369392.2:c.64_1003del
NM_001369393.2:c.64_1003del
NM_001369394.1:c.64_1003del
NM_001369394.2:c.64_1003del
NM_001386137.1:c.-218_613del
NM_001386138.1:c.-218_613del
NM_001386139.1:c.-218_613del
NM_004992.4:c.343_1282del