Canonical Allele Identifier: CA2466571634
Gene: MECP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154032467_154032472delinsTTTCTC , CM000685.2:g.154032467_154032472delinsTTTCTC GRCh38
NC_000023.10:g.153297918_153297923delinsTTTCTC , CM000685.1:g.153297918_153297923delinsTTTCTC GRCh37
NC_000023.9:g.152951112_152951117delinsTTTCTC NCBI36
NG_007107.2:g.109656_109661delinsGAGAAA
NG_007107.3:g.109632_109637delinsGAGAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000303391.11:c.112_117delinsGAGAAA MANE Plus Clinical ENSP00000301948.6:p.Glu38=
ENST00000453960.7:c.148_153delinsGAGAAA MANE Select ENSP00000395535.2:p.Glu50=
ENST00000611468.2:n.360_365delinsGAGAAA
ENST00000630151.2:c.112_117delinsGAGAAA ENSP00000486089.1:p.Glu38=
ENST00000676382.1:n.305_310delinsGAGAAA
ENST00000303391.10:c.112_117delinsGAGAAA ENSP00000301948.6:p.Glu38=
ENST00000369957.5:c.*166_*171delinsGAGAAA ENSP00000358973.4:n.*166_*171delinsGAGAAA...
ENST00000407218.5:c.148_153delinsGAGAAA ENSP00000384865.2:p.Glu50=
ENST00000415944.3:c.112_117delinsGAGAAA ENSP00000416267.1:p.Glu38=
ENST00000453960.6:c.148_153delinsGAGAAA ENSP00000395535.2:p.Glu50=
ENST00000460227.4:n.1261_1266delinsGAGAAA
ENST00000463644.5:n.1051_1056delinsGAGAAA
ENST00000481807.3:n.398_403delinsGAGAAA
ENST00000486506.5:n.2460_2465delinsGAGAAA
ENST00000488293.4:n.1161_1166delinsGAGAAA
ENST00000496908.5:n.243_248delinsGAGAAA
ENST00000611468.1:c.100_105delinsGAGAAA ENSP00000479736.1:p.Glu34=
ENST00000619732.4:c.112_117delinsGAGAAA ENSP00000480973.1:p.Glu38=
ENST00000622433.4:c.100_105delinsGAGAAA ENSP00000484470.1:p.Glu34=
ENST00000625300.1:n.337_342delinsGAGAAA
ENST00000626422.2:n.822_827delinsGAGAAA
ENST00000628176.2:c.112_117delinsGAGAAA ENSP00000486978.1:p.Glu38=
ENST00000630151.1:c.112_117delinsGAGAAA ENSP00000486089.1:p.Glu38=
ENST00000631210.1:n.391_396delinsGAGAAA
NM_001110792.1:c.148_153delinsGAGAAA NP_001104262.1:p.Glu50=
NM_001316337.1:c.-168_-163delinsGAGAAA NP_001303266.1:n.-168_-163delinsGAGAAA
NM_004992.3:c.112_117delinsGAGAAA NP_004983.1:p.Glu38=
XM_005274681.3:c.112_117delinsGAGAAA XP_005274738.1:p.Glu38=
XM_005274682.3:c.-168_-163delinsGAGAAA XP_005274739.1:n.-168_-163delinsGAGAAA
XM_005274683.3:c.-168_-163delinsGAGAAA XP_005274740.1:n.-168_-163delinsGAGAAA
XM_011531166.1:c.-168_-163delinsGAGAAA XP_011529468.1:n.-168_-163delinsGAGAAA
XM_006724819.3:c.-449_-444delinsGAGAAA XP_006724882.1:n.-449_-444delinsGAGAAA
XM_011531166.2:c.-168_-163delinsGAGAAA XP_011529468.1:n.-168_-163delinsGAGAAA
XM_024452383.1:c.-168_-163delinsGAGAAA XP_024308151.1:n.-168_-163delinsGAGAAA
XM_024452384.1:c.-168_-163delinsGAGAAA XP_024308152.1:n.-168_-163delinsGAGAAA
NM_001110792.2:c.148_153delinsGAGAAA MANE Select NP_001104262.1:p.Glu50=
NM_001316337.2:c.-168_-163delinsGAGAAA NP_001303266.1:n.-168_-163delinsGAGAAA
NM_001369391.2:c.-168_-163delinsGAGAAA NP_001356320.1:n.-168_-163delinsGAGAAA
NM_001369392.2:c.-168_-163delinsGAGAAA NP_001356321.1:n.-168_-163delinsGAGAAA
NM_001369393.2:c.-168_-163delinsGAGAAA NP_001356322.1:n.-168_-163delinsGAGAAA
NM_001369394.1:c.-168_-163delinsGAGAAA NP_001356323.1:n.-168_-163delinsGAGAAA
NM_001369394.2:c.-168_-163delinsGAGAAA NP_001356323.1:n.-168_-163delinsGAGAAA
NM_001386137.1:c.-449_-444delinsGAGAAA NP_001373066.1:n.-449_-444delinsGAGAAA
NM_001386138.1:c.-449_-444delinsGAGAAA NP_001373067.1:n.-449_-444delinsGAGAAA
NM_001386139.1:c.-449_-444delinsGAGAAA NP_001373068.1:n.-449_-444delinsGAGAAA
NM_004992.4:c.112_117delinsGAGAAA MANE Plus Clinical NP_004983.1:p.Glu38=