Canonical Allele Identifier: CA415162803

Gene: MECP2

Linked Data

• MyVariant Identifiers: chrX:g.153295825A>G (hg19) ; chrX:g.154030374A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154030374A>G , CM000685.2:g.154030374A>G	GRCh38
NC_000023.10:g.153295825A>G , CM000685.1:g.153295825A>G	GRCh37
NC_000023.9:g.152949019A>G	NCBI36
NG_007107.2:g.111754T>C
NG_007107.3:g.111730T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000303391.11:c.1454T>C MANE Plus Clinical	ENSP00000301948.6:p.Val485Ala
ENST00000453960.7:c.1490T>C MANE Select	ENSP00000395535.2:p.Val497Ala
ENST00000303391.10:c.1454T>C	ENSP00000301948.6:p.Val485Ala
ENST00000453960.6:c.1490T>C	ENSP00000395535.2:p.Val497Ala
ENST00000619732.4:c.1450T>C	ENSP00000480973.1:p.Leu484=
ENST00000628176.2:c.*826T>C	ENSP00000486978.1:n.*826T>C
NM_001110792.1:c.1490T>C	NP_001104262.1:p.Val497Ala
NM_001316337.1:c.1175T>C	NP_001303266.1:p.Val392Ala
NM_004992.3:c.1454T>C	NP_004983.1:p.Val485Ala
XM_005274681.3:c.1454T>C	XP_005274738.1:p.Val485Ala
XM_005274682.3:c.1175T>C	XP_005274739.1:p.Val392Ala
XM_005274683.3:c.1175T>C	XP_005274740.1:p.Val392Ala
XM_006724819.2:c.785T>C	XP_006724882.1:p.Val262Ala
XM_011531166.1:c.1175T>C	XP_011529468.1:p.Val392Ala
XM_006724819.3:c.785T>C	XP_006724882.1:p.Val262Ala
XM_011531166.2:c.1175T>C	XP_011529468.1:p.Val392Ala
XM_024452383.1:c.1175T>C	XP_024308151.1:p.Val392Ala
XM_024452384.1:c.1175T>C	XP_024308152.1:p.Val392Ala
NM_001110792.2:c.1490T>C MANE Select	NP_001104262.1:p.Val497Ala
NM_001316337.2:c.1175T>C	NP_001303266.1:p.Val392Ala
NM_001369391.2:c.1175T>C	NP_001356320.1:p.Val392Ala
NM_001369392.2:c.1175T>C	NP_001356321.1:p.Val392Ala
NM_001369393.2:c.1175T>C	NP_001356322.1:p.Val392Ala
NM_001369394.1:c.1175T>C	NP_001356323.1:p.Val392Ala
NM_001369394.2:c.1175T>C	NP_001356323.1:p.Val392Ala
NM_001386137.1:c.785T>C	NP_001373066.1:p.Val262Ala
NM_001386138.1:c.785T>C	NP_001373067.1:p.Val262Ala
NM_001386139.1:c.785T>C	NP_001373068.1:p.Val262Ala
NM_004992.4:c.1454T>C MANE Plus Clinical	NP_004983.1:p.Val485Ala