Canonical Allele Identifier: CA2466570878
Gene: MECP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154031201C= , CM000685.2:g.154031201C= GRCh38
NC_000023.10:g.153296652C= , CM000685.1:g.153296652C= GRCh37
NC_000023.9:g.152949846C= NCBI36
NG_007107.2:g.110927G=
NG_007107.3:g.110903G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.627G= MANE Plus Clinical ENSP00000301948.6:p.Val209=
ENST00000453960.7:c.663G= MANE Select ENSP00000395535.2:p.Val221=
ENST00000637917.1:c.65+195G=
ENST00000303391.10:c.627G= ENSP00000301948.6:p.Val209=
ENST00000407218.5:c.554G= ENSP00000384865.2:p.Ter185=
ENST00000453960.6:c.663G= ENSP00000395535.2:p.Val221=
ENST00000619732.4:c.627G= ENSP00000480973.1:p.Val209=
ENST00000622433.4:c.615G= ENSP00000484470.1:p.Val205=
ENST00000628176.2:c.518G= ENSP00000486978.1:p.Ter173=
NM_001110792.1:c.663G= NP_001104262.1:p.Val221=
NM_001316337.1:c.348G= NP_001303266.1:p.Val116=
NM_004992.3:c.627G= NP_004983.1:p.Val209=
XM_005274681.3:c.627G= XP_005274738.1:p.Val209=
XM_005274682.3:c.348G= XP_005274739.1:p.Val116=
XM_005274683.3:c.348G= XP_005274740.1:p.Val116=
XM_006724819.2:c.-43G= XP_006724882.1:n.-43G=
XM_011531166.1:c.348G= XP_011529468.1:p.Val116=
XM_006724819.3:c.-43G= XP_006724882.1:n.-43G=
XM_011531166.2:c.348G= XP_011529468.1:p.Val116=
XM_024452383.1:c.348G= XP_024308151.1:p.Val116=
XM_024452384.1:c.348G= XP_024308152.1:p.Val116=
NM_001110792.2:c.663G= MANE Select NP_001104262.1:p.Val221=
NM_001316337.2:c.348G= NP_001303266.1:p.Val116=
NM_001369391.2:c.348G= NP_001356320.1:p.Val116=
NM_001369392.2:c.348G= NP_001356321.1:p.Val116=
NM_001369393.2:c.348G= NP_001356322.1:p.Val116=
NM_001369394.1:c.348G= NP_001356323.1:p.Val116=
NM_001369394.2:c.348G= NP_001356323.1:p.Val116=
NM_001386137.1:c.-43G= NP_001373066.1:n.-43G=
NM_001386138.1:c.-43G= NP_001373067.1:n.-43G=
NM_001386139.1:c.-43G= NP_001373068.1:n.-43G=
NM_004992.4:c.627G= MANE Plus Clinical NP_004983.1:p.Val209=