Canonical Allele Identifier: CA10606762
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 290402
dbSNP Id: rs868943420

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154031208A>G , CM000685.2:g.154031208A>G GRCh38
NC_000023.10:g.153296659A>G , CM000685.1:g.153296659A>G GRCh37
NC_000023.9:g.152949853A>G NCBI36
NG_007107.2:g.110920T>C
NG_007107.3:g.110896T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.620T>C MANE Plus Clinical ENSP00000301948.6:p.Val207Ala
ENST00000453960.7:c.656T>C MANE Select ENSP00000395535.2:p.Val219Ala
ENST00000637917.1:c.65+188T>C
ENST00000303391.10:c.620T>C ENSP00000301948.6:p.Val207Ala
ENST00000407218.5:c.547T>C ENSP00000384865.2:p.Cys183Arg
ENST00000453960.6:c.656T>C ENSP00000395535.2:p.Val219Ala
ENST00000619732.4:c.620T>C ENSP00000480973.1:p.Val207Ala
ENST00000622433.4:c.608T>C ENSP00000484470.1:p.Val203Ala
ENST00000628176.2:c.511T>C ENSP00000486978.1:p.Cys171Arg
NM_001110792.1:c.656T>C NP_001104262.1:p.Val219Ala
NM_001316337.1:c.341T>C NP_001303266.1:p.Val114Ala
NM_004992.3:c.620T>C NP_004983.1:p.Val207Ala
XM_005274681.3:c.620T>C XP_005274738.1:p.Val207Ala
XM_005274682.3:c.341T>C XP_005274739.1:p.Val114Ala
XM_005274683.3:c.341T>C XP_005274740.1:p.Val114Ala
XM_006724819.2:c.-50T>C XP_006724882.1:n.-50T>C
XM_011531166.1:c.341T>C XP_011529468.1:p.Val114Ala
XM_006724819.3:c.-50T>C XP_006724882.1:n.-50T>C
XM_011531166.2:c.341T>C XP_011529468.1:p.Val114Ala
XM_024452383.1:c.341T>C XP_024308151.1:p.Val114Ala
XM_024452384.1:c.341T>C XP_024308152.1:p.Val114Ala
NM_001110792.2:c.656T>C MANE Select NP_001104262.1:p.Val219Ala
NM_001316337.2:c.341T>C NP_001303266.1:p.Val114Ala
NM_001369391.2:c.341T>C NP_001356320.1:p.Val114Ala
NM_001369392.2:c.341T>C NP_001356321.1:p.Val114Ala
NM_001369393.2:c.341T>C NP_001356322.1:p.Val114Ala
NM_001369394.1:c.341T>C NP_001356323.1:p.Val114Ala
NM_001369394.2:c.341T>C NP_001356323.1:p.Val114Ala
NM_001386137.1:c.-50T>C NP_001373066.1:n.-50T>C
NM_001386138.1:c.-50T>C NP_001373067.1:n.-50T>C
NM_001386139.1:c.-50T>C NP_001373068.1:n.-50T>C
NM_004992.4:c.620T>C MANE Plus Clinical NP_004983.1:p.Val207Ala