Canonical Allele Identifier: CA2466568735
Gene: MECP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154028145C= , CM000685.2:g.154028145C= GRCh38
NC_000023.10:g.153293596C= , CM000685.1:g.153293596C= GRCh37
NC_000023.9:g.152946790C= NCBI36
NG_007107.2:g.113983G=
NG_007107.3:g.113959G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.*2222G= MANE Plus Clinical ENSP00000301948.6:n.*2222G=
ENST00000453960.7:c.*2222G= MANE Select ENSP00000395535.2:n.*2222G=
ENST00000303391.10:c.*2222G= ENSP00000301948.6:n.*2222G=
ENST00000619732.4:c.*2149G= ENSP00000480973.1:n.*2149G=
NM_004992.3:c.*2222G= NP_004983.1:n.*2222G=
XM_006724819.3:c.*2222G= XP_006724882.1:n.*2222G=
XM_011531166.2:c.*2222G= XP_011529468.1:n.*2222G=
XM_024452383.1:c.*2222G= XP_024308151.1:n.*2222G=
XM_024452384.1:c.*2222G= XP_024308152.1:n.*2222G=
NM_001110792.2:c.*2222G= MANE Select NP_001104262.1:n.*2222G=
NM_001316337.2:c.*2222G= NP_001303266.1:n.*2222G=
NM_001369391.2:c.*2222G= NP_001356320.1:n.*2222G=
NM_001369392.2:c.*2222G= NP_001356321.1:n.*2222G=
NM_001369393.2:c.*2222G= NP_001356322.1:n.*2222G=
NM_001369394.2:c.*2222G= NP_001356323.1:n.*2222G=
NM_001386137.1:c.*2222G= NP_001373066.1:n.*2222G=
NM_001386138.1:c.*2222G= NP_001373067.1:n.*2222G=
NM_001386139.1:c.*2222G= NP_001373068.1:n.*2222G=
NM_004992.4:c.*2222G= MANE Plus Clinical NP_004983.1:n.*2222G=
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