Canonical Allele Identifier: CA415162270

Gene: MECP2

Linked Data

• dbSNP Id: rs2065899215
• MyVariant Identifiers: chrX:g.153295800A>C (hg19) ; chrX:g.154030349A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154030349A>C , CM000685.2:g.154030349A>C	GRCh38
NC_000023.10:g.153295800A>C , CM000685.1:g.153295800A>C	GRCh37
NC_000023.9:g.152948994A>C	NCBI36
NG_007107.2:g.111779T>G
NG_007107.3:g.111755T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303391.11:c.*18T>G MANE Plus Clinical	ENSP00000301948.6:n.*18T>G
ENST00000453960.7:c.*18T>G MANE Select	ENSP00000395535.2:n.*18T>G
ENST00000303391.10:c.*18T>G	ENSP00000301948.6:n.*18T>G
ENST00000453960.6:c.*18T>G	ENSP00000395535.2:n.*18T>G
ENST00000619732.4:c.1475T>G	ENSP00000480973.1:p.Leu492Trp
ENST00000628176.2:c.*851T>G	ENSP00000486978.1:n.*851T>G
NM_001110792.1:c.*18T>G	NP_001104262.1:n.*18T>G
NM_001316337.1:c.*18T>G	NP_001303266.1:n.*18T>G
NM_004992.3:c.*18T>G	NP_004983.1:n.*18T>G
XM_005274681.3:c.*18T>G	XP_005274738.1:n.*18T>G
XM_005274682.3:c.*18T>G	XP_005274739.1:n.*18T>G
XM_005274683.3:c.*18T>G	XP_005274740.1:n.*18T>G
XM_006724819.2:c.*18T>G	XP_006724882.1:n.*18T>G
XM_011531166.1:c.*18T>G	XP_011529468.1:n.*18T>G
XM_006724819.3:c.*18T>G	XP_006724882.1:n.*18T>G
XM_011531166.2:c.*18T>G	XP_011529468.1:n.*18T>G
XM_024452383.1:c.*18T>G	XP_024308151.1:n.*18T>G
XM_024452384.1:c.*18T>G	XP_024308152.1:n.*18T>G
NM_001110792.2:c.*18T>G MANE Select	NP_001104262.1:n.*18T>G
NM_001316337.2:c.*18T>G	NP_001303266.1:n.*18T>G
NM_001369391.2:c.*18T>G	NP_001356320.1:n.*18T>G
NM_001369392.2:c.*18T>G	NP_001356321.1:n.*18T>G
NM_001369393.2:c.*18T>G	NP_001356322.1:n.*18T>G
NM_001369394.1:c.*18T>G	NP_001356323.1:n.*18T>G
NM_001369394.2:c.*18T>G	NP_001356323.1:n.*18T>G
NM_001386137.1:c.*18T>G	NP_001373066.1:n.*18T>G
NM_001386138.1:c.*18T>G	NP_001373067.1:n.*18T>G
NM_001386139.1:c.*18T>G	NP_001373068.1:n.*18T>G
NM_004992.4:c.*18T>G MANE Plus Clinical	NP_004983.1:n.*18T>G