Canonical Allele Identifier: CA274628
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143585
dbSNP Id: rs61748410

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154031359A>T , CM000685.2:g.154031359A>T GRCh38
NC_000023.10:g.153296810A>T , CM000685.1:g.153296810A>T GRCh37
NC_000023.9:g.152950004A>T NCBI36
NG_007107.2:g.110769T>A
NG_007107.3:g.110745T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.469T>A MANE Plus Clinical ENSP00000301948.6:p.Phe157Ile
ENST00000453960.7:c.505T>A MANE Select ENSP00000395535.2:p.Phe169Ile
ENST00000637917.1:c.65+37T>A
ENST00000303391.10:c.469T>A ENSP00000301948.6:p.Phe157Ile
ENST00000407218.5:c.468+37T>A ENSP00000384865.2:n.468+37T>A
ENST00000453960.6:c.505T>A ENSP00000395535.2:p.Phe169Ile
ENST00000486506.5:n.2817T>A
ENST00000611468.1:c.457T>A ENSP00000479736.1:p.Phe153Ile
ENST00000619732.4:c.469T>A ENSP00000480973.1:p.Phe157Ile
ENST00000622433.4:c.457T>A ENSP00000484470.1:p.Phe153Ile
ENST00000628176.2:c.432+37T>A ENSP00000486978.1:n.432+37T>A
NM_001110792.1:c.505T>A NP_001104262.1:p.Phe169Ile
NM_001316337.1:c.190T>A NP_001303266.1:p.Phe64Ile
NM_004992.3:c.469T>A NP_004983.1:p.Phe157Ile
XM_005274681.3:c.469T>A XP_005274738.1:p.Phe157Ile
XM_005274682.3:c.190T>A XP_005274739.1:p.Phe64Ile
XM_005274683.3:c.190T>A XP_005274740.1:p.Phe64Ile
XM_006724819.2:c.-129+37T>A XP_006724882.1:n.-129+37T>A
XM_011531166.1:c.190T>A XP_011529468.1:p.Phe64Ile
XM_006724819.3:c.-129+37T>A XP_006724882.1:n.-129+37T>A
XM_011531166.2:c.190T>A XP_011529468.1:p.Phe64Ile
XM_024452383.1:c.190T>A XP_024308151.1:p.Phe64Ile
XM_024452384.1:c.190T>A XP_024308152.1:p.Phe64Ile
NM_001110792.2:c.505T>A MANE Select NP_001104262.1:p.Phe169Ile
NM_001316337.2:c.190T>A NP_001303266.1:p.Phe64Ile
NM_001369391.2:c.190T>A NP_001356320.1:p.Phe64Ile
NM_001369392.2:c.190T>A NP_001356321.1:p.Phe64Ile
NM_001369393.2:c.190T>A NP_001356322.1:p.Phe64Ile
NM_001369394.1:c.190T>A NP_001356323.1:p.Phe64Ile
NM_001369394.2:c.190T>A NP_001356323.1:p.Phe64Ile
NM_001386137.1:c.-129+37T>A NP_001373066.1:n.-129+37T>A
NM_001386138.1:c.-129+37T>A NP_001373067.1:n.-129+37T>A
NM_001386139.1:c.-129+37T>A NP_001373068.1:n.-129+37T>A
NM_004992.4:c.469T>A MANE Plus Clinical NP_004983.1:p.Phe157Ile