Canonical Allele Identifier: CA2466571606
Gene: MECP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154032393_154032395delinsGTC , CM000685.2:g.154032393_154032395delinsGTC GRCh38
NC_000023.10:g.153297844_153297846delinsGTC , CM000685.1:g.153297844_153297846delinsGTC GRCh37
NC_000023.9:g.152951038_152951040delinsGTC NCBI36
NG_007107.2:g.109733_109735delinsGAC
NG_007107.3:g.109709_109711delinsGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.189_191delinsGAC MANE Plus Clinical ENSP00000301948.6:p.Glu63=
ENST00000453960.7:c.225_227delinsGAC MANE Select ENSP00000395535.2:p.Glu75=
ENST00000303391.10:c.189_191delinsGAC ENSP00000301948.6:p.Glu63=
ENST00000369957.5:c.*243_*245delinsGAC ENSP00000358973.4:n.*243_*245delinsGAC
ENST00000407218.5:c.225_227delinsGAC ENSP00000384865.2:p.Glu75=
ENST00000453960.6:c.225_227delinsGAC ENSP00000395535.2:p.Glu75=
ENST00000486506.5:n.2537_2539delinsGAC
ENST00000496908.5:n.320_322delinsGAC
ENST00000611468.1:c.177_179delinsGAC ENSP00000479736.1:p.Glu59=
ENST00000619732.4:c.189_191delinsGAC ENSP00000480973.1:p.Glu63=
ENST00000622433.4:c.177_179delinsGAC ENSP00000484470.1:p.Glu59=
ENST00000628176.2:c.189_191delinsGAC ENSP00000486978.1:p.Glu63=
ENST00000631210.1:n.468_470delinsGAC
NM_001110792.1:c.225_227delinsGAC NP_001104262.1:p.Glu75=
NM_001316337.1:c.-91_-89delinsGAC NP_001303266.1:n.-91_-89delinsGAC
NM_004992.3:c.189_191delinsGAC NP_004983.1:p.Glu63=
XM_005274681.3:c.189_191delinsGAC XP_005274738.1:p.Glu63=
XM_005274682.3:c.-91_-89delinsGAC XP_005274739.1:n.-91_-89delinsGAC
XM_005274683.3:c.-91_-89delinsGAC XP_005274740.1:n.-91_-89delinsGAC
XM_011531166.1:c.-91_-89delinsGAC XP_011529468.1:n.-91_-89delinsGAC
XM_006724819.3:c.-372_-370delinsGAC XP_006724882.1:n.-372_-370delinsGAC
XM_011531166.2:c.-91_-89delinsGAC XP_011529468.1:n.-91_-89delinsGAC
XM_024452383.1:c.-91_-89delinsGAC XP_024308151.1:n.-91_-89delinsGAC
XM_024452384.1:c.-91_-89delinsGAC XP_024308152.1:n.-91_-89delinsGAC
NM_001110792.2:c.225_227delinsGAC MANE Select NP_001104262.1:p.Glu75=
NM_001316337.2:c.-91_-89delinsGAC NP_001303266.1:n.-91_-89delinsGAC
NM_001369391.2:c.-91_-89delinsGAC NP_001356320.1:n.-91_-89delinsGAC
NM_001369392.2:c.-91_-89delinsGAC NP_001356321.1:n.-91_-89delinsGAC
NM_001369393.2:c.-91_-89delinsGAC NP_001356322.1:n.-91_-89delinsGAC
NM_001369394.1:c.-91_-89delinsGAC NP_001356323.1:n.-91_-89delinsGAC
NM_001369394.2:c.-91_-89delinsGAC NP_001356323.1:n.-91_-89delinsGAC
NM_001386137.1:c.-372_-370delinsGAC NP_001373066.1:n.-372_-370delinsGAC
NM_001386138.1:c.-372_-370delinsGAC NP_001373067.1:n.-372_-370delinsGAC
NM_001386139.1:c.-372_-370delinsGAC NP_001373068.1:n.-372_-370delinsGAC
NM_004992.4:c.189_191delinsGAC MANE Plus Clinical NP_004983.1:p.Glu63=