Canonical Allele Identifier: CA270411
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143569
ClinVar RCV Id: RCV000133104 RCV001849959
dbSNP Id: rs61748395
MyVariant Identifiers: chrX:g.153296857T>C (hg19) chrX:g.154031406T>C (hg38)
PubMed: PMID:15173251 PMID:16473305 PMID:16879196
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154031406T>C , CM000685.2:g.154031406T>C GRCh38
NC_000023.10:g.153296857T>C , CM000685.1:g.153296857T>C GRCh37
NC_000023.9:g.152950051T>C NCBI36
NG_007107.2:g.110722A>G
NG_007107.3:g.110698A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.422A>G MANE Plus Clinical ENSP00000301948.6:p.Tyr141Cys
ENST00000453960.7:c.458A>G MANE Select ENSP00000395535.2:p.Tyr153Cys
ENST00000637917.1:c.55A>G
ENST00000303391.10:c.422A>G ENSP00000301948.6:p.Tyr141Cys
ENST00000369957.5:c.*476A>G ENSP00000358973.4:n.*476A>G
ENST00000407218.5:c.458A>G ENSP00000384865.2:p.Tyr153Cys
ENST00000453960.6:c.458A>G ENSP00000395535.2:p.Tyr153Cys
ENST00000486506.5:n.2770A>G
ENST00000611468.1:c.410A>G ENSP00000479736.1:p.Tyr137Cys
ENST00000619732.4:c.422A>G ENSP00000480973.1:p.Tyr141Cys
ENST00000622433.4:c.410A>G ENSP00000484470.1:p.Tyr137Cys
ENST00000628176.2:c.422A>G ENSP00000486978.1:p.Tyr141Cys
NM_001110792.1:c.458A>G NP_001104262.1:p.Tyr153Cys
NM_001316337.1:c.143A>G NP_001303266.1:p.Tyr48Cys
NM_004992.3:c.422A>G NP_004983.1:p.Tyr141Cys
XM_005274681.3:c.422A>G XP_005274738.1:p.Tyr141Cys
XM_005274682.3:c.143A>G XP_005274739.1:p.Tyr48Cys
XM_005274683.3:c.143A>G XP_005274740.1:p.Tyr48Cys
XM_006724819.2:c.-139A>G XP_006724882.1:n.-139A>G
XM_011531166.1:c.143A>G XP_011529468.1:p.Tyr48Cys
XM_006724819.3:c.-139A>G XP_006724882.1:n.-139A>G
XM_011531166.2:c.143A>G XP_011529468.1:p.Tyr48Cys
XM_024452383.1:c.143A>G XP_024308151.1:p.Tyr48Cys
XM_024452384.1:c.143A>G XP_024308152.1:p.Tyr48Cys
NM_001110792.2:c.458A>G MANE Select NP_001104262.1:p.Tyr153Cys
NM_001316337.2:c.143A>G NP_001303266.1:p.Tyr48Cys
NM_001369391.2:c.143A>G NP_001356320.1:p.Tyr48Cys
NM_001369392.2:c.143A>G NP_001356321.1:p.Tyr48Cys
NM_001369393.2:c.143A>G NP_001356322.1:p.Tyr48Cys
NM_001369394.1:c.143A>G NP_001356323.1:p.Tyr48Cys
NM_001369394.2:c.143A>G NP_001356323.1:p.Tyr48Cys
NM_001386137.1:c.-139A>G NP_001373066.1:n.-139A>G
NM_001386138.1:c.-139A>G NP_001373067.1:n.-139A>G
NM_001386139.1:c.-139A>G NP_001373068.1:n.-139A>G
NM_004992.4:c.422A>G MANE Plus Clinical NP_004983.1:p.Tyr141Cys
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