Canonical Allele Identifier: CA337261655
Gene: MECP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154030276G>A , CM000685.2:g.154030276G>A GRCh38
NC_000023.10:g.153295727G>A , CM000685.1:g.153295727G>A GRCh37
NC_000023.9:g.152948921G>A NCBI36
NG_007107.2:g.111852C>T
NG_007107.3:g.111828C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.*91C>T MANE Plus Clinical ENSP00000301948.6:n.*91C>T
ENST00000453960.7:c.*91C>T MANE Select ENSP00000395535.2:n.*91C>T
ENST00000303391.10:c.*91C>T ENSP00000301948.6:n.*91C>T
ENST00000453960.6:c.*91C>T ENSP00000395535.2:n.*91C>T
ENST00000619732.4:c.*18C>T ENSP00000480973.1:n.*18C>T
ENST00000628176.2:c.*924C>T ENSP00000486978.1:n.*924C>T
NM_001110792.1:c.*91C>T NP_001104262.1:n.*91C>T
NM_001316337.1:c.*91C>T NP_001303266.1:n.*91C>T
NM_004992.3:c.*91C>T NP_004983.1:n.*91C>T
XM_005274681.3:c.*91C>T XP_005274738.1:n.*91C>T
XM_005274682.3:c.*91C>T XP_005274739.1:n.*91C>T
XM_005274683.3:c.*91C>T XP_005274740.1:n.*91C>T
XM_006724819.2:c.*91C>T XP_006724882.1:n.*91C>T
XM_011531166.1:c.*91C>T XP_011529468.1:n.*91C>T
XM_006724819.3:c.*91C>T XP_006724882.1:n.*91C>T
XM_011531166.2:c.*91C>T XP_011529468.1:n.*91C>T
XM_024452383.1:c.*91C>T XP_024308151.1:n.*91C>T
XM_024452384.1:c.*91C>T XP_024308152.1:n.*91C>T
NM_001110792.2:c.*91C>T MANE Select NP_001104262.1:n.*91C>T
NM_001316337.2:c.*91C>T NP_001303266.1:n.*91C>T
NM_001369391.2:c.*91C>T NP_001356320.1:n.*91C>T
NM_001369392.2:c.*91C>T NP_001356321.1:n.*91C>T
NM_001369393.2:c.*91C>T NP_001356322.1:n.*91C>T
NM_001369394.1:c.*91C>T NP_001356323.1:n.*91C>T
NM_001369394.2:c.*91C>T NP_001356323.1:n.*91C>T
NM_001386137.1:c.*91C>T NP_001373066.1:n.*91C>T
NM_001386138.1:c.*91C>T NP_001373067.1:n.*91C>T
NM_001386139.1:c.*91C>T NP_001373068.1:n.*91C>T
NM_004992.4:c.*91C>T MANE Plus Clinical NP_004983.1:n.*91C>T
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