Canonical Allele Identifier: CA915952034
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 813009
ClinVar RCV Id: RCV001004017
dbSNP Id: rs1603310867

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154032472_154032476del , CM000685.2:g.154032472_154032476del GRCh38
NC_000023.10:g.153297923_153297927del , CM000685.1:g.153297923_153297927del GRCh37
NC_000023.9:g.152951117_152951121del NCBI36
NG_007107.2:g.109656_109660del
NG_007107.3:g.109632_109636del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.112_116del MANE Plus Clinical ENSP00000301948.6:p.Glu38ArgfsTer5
ENST00000453960.7:c.148_152del MANE Select ENSP00000395535.2:p.Glu50ArgfsTer5
ENST00000611468.2:n.360_364del
ENST00000630151.2:c.112_116del ENSP00000486089.1:p.Glu38ArgfsTer?
ENST00000676382.1:n.305_309del
ENST00000303391.10:c.112_116del ENSP00000301948.6:p.Glu38ArgfsTer5
ENST00000369957.5:c.*166_*170del ENSP00000358973.4:n.*166_*170del
ENST00000407218.5:c.148_152del ENSP00000384865.2:p.Glu50ArgfsTer5
ENST00000415944.3:c.112_116del ENSP00000416267.1:p.Glu38ArgfsTer5
ENST00000453960.6:c.148_152del ENSP00000395535.2:p.Glu50ArgfsTer5
ENST00000460227.4:n.1261_1265del
ENST00000463644.5:n.1051_1055del
ENST00000481807.3:n.398_402del
ENST00000486506.5:n.2460_2464del
ENST00000488293.4:n.1161_1165del
ENST00000496908.5:n.243_247del
ENST00000611468.1:c.100_104del ENSP00000479736.1:p.Glu34ArgfsTer5
ENST00000619732.4:c.112_116del ENSP00000480973.1:p.Glu38ArgfsTer5
ENST00000622433.4:c.100_104del ENSP00000484470.1:p.Glu34ArgfsTer5
ENST00000625300.1:n.337_341del
ENST00000626422.2:n.822_826del
ENST00000628176.2:c.112_116del ENSP00000486978.1:p.Glu38ArgfsTer5
ENST00000630151.1:c.112_116del ENSP00000486089.1:p.Glu38ArgfsTer?
ENST00000631210.1:n.391_395del
NM_001110792.1:c.148_152del NP_001104262.1:p.Glu50ArgfsTer5
NM_001316337.1:c.-168_-164del NP_001303266.1:n.-168_-164del
NM_004992.3:c.112_116del NP_004983.1:p.Glu38ArgfsTer5
XM_005274681.3:c.112_116del XP_005274738.1:p.Glu38ArgfsTer5
XM_005274682.3:c.-168_-164del XP_005274739.1:n.-168_-164del
XM_005274683.3:c.-168_-164del XP_005274740.1:n.-168_-164del
XM_011531166.1:c.-168_-164del XP_011529468.1:n.-168_-164del
XM_006724819.3:c.-449_-445del XP_006724882.1:n.-449_-445del
XM_011531166.2:c.-168_-164del XP_011529468.1:n.-168_-164del
XM_024452383.1:c.-168_-164del XP_024308151.1:n.-168_-164del
XM_024452384.1:c.-168_-164del XP_024308152.1:n.-168_-164del
NM_001110792.2:c.148_152del MANE Select NP_001104262.1:p.Glu50ArgfsTer5
NM_001316337.2:c.-168_-164del NP_001303266.1:n.-168_-164del
NM_001369391.2:c.-168_-164del NP_001356320.1:n.-168_-164del
NM_001369392.2:c.-168_-164del NP_001356321.1:n.-168_-164del
NM_001369393.2:c.-168_-164del NP_001356322.1:n.-168_-164del
NM_001369394.1:c.-168_-164del NP_001356323.1:n.-168_-164del
NM_001369394.2:c.-168_-164del NP_001356323.1:n.-168_-164del
NM_001386137.1:c.-449_-445del NP_001373066.1:n.-449_-445del
NM_001386138.1:c.-449_-445del NP_001373067.1:n.-449_-445del
NM_001386139.1:c.-449_-445del NP_001373068.1:n.-449_-445del
NM_004992.4:c.112_116del MANE Plus Clinical NP_004983.1:p.Glu38ArgfsTer5