Canonical Allele Identifier: CA415178185

Gene: MECP2

Linked Data

• MyVariant Identifiers: chrX:g.153297914C>G (hg19) ; chrX:g.154032463C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154032463C>G , CM000685.2:g.154032463C>G	GRCh38
NC_000023.10:g.153297914C>G , CM000685.1:g.153297914C>G	GRCh37
NC_000023.9:g.152951108C>G	NCBI36
NG_007107.2:g.109665G>C
NG_007107.3:g.109641G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303391.11:c.121G>C MANE Plus Clinical	ENSP00000301948.6:p.Gly41Arg
ENST00000453960.7:c.157G>C MANE Select	ENSP00000395535.2:p.Gly53Arg
ENST00000630151.2:c.121G>C	ENSP00000486089.1:p.Gly41Arg
ENST00000303391.10:c.121G>C	ENSP00000301948.6:p.Gly41Arg
ENST00000369957.5:c.*175G>C	ENSP00000358973.4:n.*175G>C
ENST00000407218.5:c.157G>C	ENSP00000384865.2:p.Gly53Arg
ENST00000415944.3:c.121G>C	ENSP00000416267.1:p.Gly41Arg
ENST00000453960.6:c.157G>C	ENSP00000395535.2:p.Gly53Arg
ENST00000460227.4:n.1270G>C
ENST00000463644.5:n.1060G>C
ENST00000481807.3:n.407G>C
ENST00000486506.5:n.2469G>C
ENST00000488293.4:n.1170G>C
ENST00000496908.5:n.252G>C
ENST00000611468.1:c.109G>C	ENSP00000479736.1:p.Gly37Arg
ENST00000619732.4:c.121G>C	ENSP00000480973.1:p.Gly41Arg
ENST00000622433.4:c.109G>C	ENSP00000484470.1:p.Gly37Arg
ENST00000625300.1:n.346G>C
ENST00000626422.2:n.831G>C
ENST00000628176.2:c.121G>C	ENSP00000486978.1:p.Gly41Arg
ENST00000630151.1:c.121G>C	ENSP00000486089.1:p.Gly41Arg
ENST00000631210.1:n.400G>C
NM_001110792.1:c.157G>C	NP_001104262.1:p.Gly53Arg
NM_001316337.1:c.-159G>C	NP_001303266.1:n.-159G>C
NM_004992.3:c.121G>C	NP_004983.1:p.Gly41Arg
XM_005274681.3:c.121G>C	XP_005274738.1:p.Gly41Arg
XM_005274682.3:c.-159G>C	XP_005274739.1:n.-159G>C
XM_005274683.3:c.-159G>C	XP_005274740.1:n.-159G>C
XM_011531166.1:c.-159G>C	XP_011529468.1:n.-159G>C
XM_006724819.3:c.-440G>C	XP_006724882.1:n.-440G>C
XM_011531166.2:c.-159G>C	XP_011529468.1:n.-159G>C
XM_024452383.1:c.-159G>C	XP_024308151.1:n.-159G>C
XM_024452384.1:c.-159G>C	XP_024308152.1:n.-159G>C
NM_001110792.2:c.157G>C MANE Select	NP_001104262.1:p.Gly53Arg
NM_001316337.2:c.-159G>C	NP_001303266.1:n.-159G>C
NM_001369391.2:c.-159G>C	NP_001356320.1:n.-159G>C
NM_001369392.2:c.-159G>C	NP_001356321.1:n.-159G>C
NM_001369393.2:c.-159G>C	NP_001356322.1:n.-159G>C
NM_001369394.1:c.-159G>C	NP_001356323.1:n.-159G>C
NM_001369394.2:c.-159G>C	NP_001356323.1:n.-159G>C
NM_001386137.1:c.-440G>C	NP_001373066.1:n.-440G>C
NM_001386138.1:c.-440G>C	NP_001373067.1:n.-440G>C
NM_001386139.1:c.-440G>C	NP_001373068.1:n.-440G>C
NM_004992.4:c.121G>C MANE Plus Clinical	NP_004983.1:p.Gly41Arg