Canonical Allele Identifier: CA1139667837
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 974859
ClinVar RCV Id: RCV001251144
dbSNP Id: rs2065988707

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154032442_154032445dup , CM000685.2:g.154032442_154032445dup GRCh38
NC_000023.10:g.153297893_153297896dup , CM000685.1:g.153297893_153297896dup GRCh37
NC_000023.9:g.152951087_152951090dup NCBI36
NG_007107.2:g.109685_109688dup
NG_007107.3:g.109661_109664dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.141_144dup MANE Plus Clinical ENSP00000301948.6:p.Ser49AlafsTer8
ENST00000453960.7:c.177_180dup MANE Select ENSP00000395535.2:p.Ser61AlafsTer8
ENST00000303391.10:c.141_144dup ENSP00000301948.6:p.Ser49AlafsTer8
ENST00000369957.5:c.*195_*198dup ENSP00000358973.4:n.*195_*198dup
ENST00000407218.5:c.177_180dup ENSP00000384865.2:p.Ser61AlafsTer8
ENST00000415944.3:c.141_144dup ENSP00000416267.1:p.Ser49AlafsTer?
ENST00000453960.6:c.177_180dup ENSP00000395535.2:p.Ser61AlafsTer8
ENST00000460227.4:n.1290_1293dup
ENST00000463644.5:n.1080_1083dup
ENST00000481807.3:n.427_430dup
ENST00000486506.5:n.2489_2492dup
ENST00000488293.4:n.1190_1193dup
ENST00000496908.5:n.272_275dup
ENST00000611468.1:c.129_132dup ENSP00000479736.1:p.Ser45AlafsTer8
ENST00000619732.4:c.141_144dup ENSP00000480973.1:p.Ser49AlafsTer8
ENST00000622433.4:c.129_132dup ENSP00000484470.1:p.Ser45AlafsTer8
ENST00000628176.2:c.141_144dup ENSP00000486978.1:p.Ser49AlafsTer8
ENST00000631210.1:n.420_423dup
NM_001110792.1:c.177_180dup NP_001104262.1:p.Ser61AlafsTer8
NM_001316337.1:c.-139_-136dup NP_001303266.1:n.-139_-136dup
NM_004992.3:c.141_144dup NP_004983.1:p.Ser49AlafsTer8
XM_005274681.3:c.141_144dup XP_005274738.1:p.Ser49AlafsTer8
XM_005274682.3:c.-139_-136dup XP_005274739.1:n.-139_-136dup
XM_005274683.3:c.-139_-136dup XP_005274740.1:n.-139_-136dup
XM_011531166.1:c.-139_-136dup XP_011529468.1:n.-139_-136dup
XM_006724819.3:c.-420_-417dup XP_006724882.1:n.-420_-417dup
XM_011531166.2:c.-139_-136dup XP_011529468.1:n.-139_-136dup
XM_024452383.1:c.-139_-136dup XP_024308151.1:n.-139_-136dup
XM_024452384.1:c.-139_-136dup XP_024308152.1:n.-139_-136dup
NM_001110792.2:c.177_180dup MANE Select NP_001104262.1:p.Ser61AlafsTer8
NM_001316337.2:c.-139_-136dup NP_001303266.1:n.-139_-136dup
NM_001369391.2:c.-139_-136dup NP_001356320.1:n.-139_-136dup
NM_001369392.2:c.-139_-136dup NP_001356321.1:n.-139_-136dup
NM_001369393.2:c.-139_-136dup NP_001356322.1:n.-139_-136dup
NM_001369394.1:c.-139_-136dup NP_001356323.1:n.-139_-136dup
NM_001369394.2:c.-139_-136dup NP_001356323.1:n.-139_-136dup
NM_001386137.1:c.-420_-417dup NP_001373066.1:n.-420_-417dup
NM_001386138.1:c.-420_-417dup NP_001373067.1:n.-420_-417dup
NM_001386139.1:c.-420_-417dup NP_001373068.1:n.-420_-417dup
NM_004992.4:c.141_144dup MANE Plus Clinical NP_004983.1:p.Ser49AlafsTer8