Canonical Allele Identifier: CA2466583260
Community Standard Title: NM_001110792.2(MECP2):c.62+32135T=
Gene: MECP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154065469A= , CM000685.2:g.154065469A= GRCh38
NC_000023.10:g.153330920A= , CM000685.1:g.153330920A= GRCh37
NC_000023.9:g.152984114A= NCBI36
NG_007107.2:g.76659T=
NG_007107.3:g.76635T=

Transcript Alleles

HGVS Amino-acid Change
NM_001110792.2:c.62+32135T= MANE Select NP_001104262.1:n.62+32135T=
ENST00000453960.7:c.62+32135T= MANE Select ENSP00000395535.2:n.62+32135T=
NM_004992.4:c.26+26715T= MANE Plus Clinical NP_004983.1:n.26+26715T=
ENST00000303391.11:c.26+26715T= MANE Plus Clinical ENSP00000301948.6:n.26+26715T=
NM_001110792.1:c.62+32135T= NP_001104262.1:n.62+32135T=
NM_001316337.1:c.-421-6903T= NP_001303266.1:n.-421-6903T=
NM_001316337.2:c.-421-6903T= NP_001303266.1:n.-421-6903T=
NM_001369391.2:c.-716-6947T= NP_001356320.1:n.-716-6947T=
NM_001369392.2:c.-365-25566T= NP_001356321.1:n.-365-25566T=
NM_001369393.2:c.-365-25566T= NP_001356322.1:n.-365-25566T=
NM_001369394.1:c.-254+31344T= NP_001356323.1:n.-254+31344T=
NM_001369394.2:c.-254+31344T= NP_001356323.1:n.-254+31344T=
NM_001386137.1:c.-646-25566T= NP_001373066.1:n.-646-25566T=
NM_001386138.1:c.-535+26715T= NP_001373067.1:n.-535+26715T=
NM_001386139.1:c.-535+32135T= NP_001373068.1:n.-535+32135T=
NM_004992.3:c.26+26715T= NP_004983.1:n.26+26715T=
ENST00000303391.10:c.26+26715T= ENSP00000301948.6:n.26+26715T=
ENST00000369957.5:c.27-6903T= ENSP00000358973.4:n.27-6903T=
ENST00000407218.5:c.62+32135T= ENSP00000384865.2:n.62+32135T=
ENST00000415944.3:c.26+26715T= ENSP00000416267.1:n.26+26715T=
ENST00000453960.6:c.62+32135T= ENSP00000395535.2:n.62+32135T=
ENST00000496908.5:n.157+31344T=
ENST00000611468.1:c.14+26715T= ENSP00000479736.1:n.14+26715T=
ENST00000611468.2:n.125-6921T=
ENST00000619732.4:c.26+26715T= ENSP00000480973.1:n.26+26715T=
ENST00000622433.4:c.14+26715T= ENSP00000484470.1:n.14+26715T=
ENST00000628176.2:c.26+26715T= ENSP00000486978.1:n.26+26715T=
ENST00000630151.1:c.26+26715T= ENSP00000486089.1:n.26+26715T=
ENST00000630151.2:c.26+26715T= ENSP00000486089.1:n.26+26715T=
ENST00000631210.1:n.306-32912T=
ENST00000637533.1:n.57+31500T=
ENST00000637791.1:n.78+26715T=
ENST00000674996.1:c.27-6947T= ENSP00000502832.1:n.27-6947T=
ENST00000675526.1:c.143-6947T= ENSP00000501710.1:n.143-6947T=
ENST00000675841.1:n.125-6947T=
ENST00000676382.1:n.23-31834T=
ENST00000700484.1:n.23-25566T=
XM_005274681.3:c.26+26715T= XP_005274738.1:n.26+26715T=
XM_005274682.3:c.-365-25566T= XP_005274739.1:n.-365-25566T=
XM_024452383.1:c.-791-6947T= XP_024308151.1:n.-791-6947T=
XM_024452384.1:c.-365-25566T= XP_024308152.1:n.-365-25566T=