Canonical Allele Identifier: CA2466571628

Gene: MECP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154032459_154032463delinsTTGCC , CM000685.2:g.154032459_154032463delinsTTGCC	GRCh38
NC_000023.10:g.153297910_153297914delinsTTGCC , CM000685.1:g.153297910_153297914delinsTTGCC	GRCh37
NC_000023.9:g.152951104_152951108delinsTTGCC	NCBI36
NG_007107.2:g.109665_109669delinsGGCAA
NG_007107.3:g.109641_109645delinsGGCAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000303391.11:c.121_125delinsGGCAA MANE Plus Clinical	ENSP00000301948.6:p.Gly41=
ENST00000453960.7:c.157_161delinsGGCAA MANE Select	ENSP00000395535.2:p.Gly53=
ENST00000630151.2:c.121_125delinsGGCAA	ENSP00000486089.1:p.Gly41=
ENST00000303391.10:c.121_125delinsGGCAA	ENSP00000301948.6:p.Gly41=
ENST00000369957.5:c.*175_*179delinsGGCAA	ENSP00000358973.4:n.*175_*179delinsGGCAA
ENST00000407218.5:c.157_161delinsGGCAA	ENSP00000384865.2:p.Gly53=
ENST00000415944.3:c.121_125delinsGGCAA	ENSP00000416267.1:p.Gly41=
ENST00000453960.6:c.157_161delinsGGCAA	ENSP00000395535.2:p.Gly53=
ENST00000460227.4:n.1270_1274delinsGGCAA
ENST00000463644.5:n.1060_1064delinsGGCAA
ENST00000481807.3:n.407_411delinsGGCAA
ENST00000486506.5:n.2469_2473delinsGGCAA
ENST00000488293.4:n.1170_1174delinsGGCAA
ENST00000496908.5:n.252_256delinsGGCAA
ENST00000611468.1:c.109_113delinsGGCAA	ENSP00000479736.1:p.Gly37=
ENST00000619732.4:c.121_125delinsGGCAA	ENSP00000480973.1:p.Gly41=
ENST00000622433.4:c.109_113delinsGGCAA	ENSP00000484470.1:p.Gly37=
ENST00000625300.1:n.346_350delinsGGCAA
ENST00000626422.2:n.831_835delinsGGCAA
ENST00000628176.2:c.121_125delinsGGCAA	ENSP00000486978.1:p.Gly41=
ENST00000630151.1:c.121_125delinsGGCAA	ENSP00000486089.1:p.Gly41=
ENST00000631210.1:n.400_404delinsGGCAA
NM_001110792.1:c.157_161delinsGGCAA	NP_001104262.1:p.Gly53=
NM_001316337.1:c.-159_-155delinsGGCAA	NP_001303266.1:n.-159_-155delinsGGCAA
NM_004992.3:c.121_125delinsGGCAA	NP_004983.1:p.Gly41=
XM_005274681.3:c.121_125delinsGGCAA	XP_005274738.1:p.Gly41=
XM_005274682.3:c.-159_-155delinsGGCAA	XP_005274739.1:n.-159_-155delinsGGCAA
XM_005274683.3:c.-159_-155delinsGGCAA	XP_005274740.1:n.-159_-155delinsGGCAA
XM_011531166.1:c.-159_-155delinsGGCAA	XP_011529468.1:n.-159_-155delinsGGCAA
XM_006724819.3:c.-440_-436delinsGGCAA	XP_006724882.1:n.-440_-436delinsGGCAA
XM_011531166.2:c.-159_-155delinsGGCAA	XP_011529468.1:n.-159_-155delinsGGCAA
XM_024452383.1:c.-159_-155delinsGGCAA	XP_024308151.1:n.-159_-155delinsGGCAA
XM_024452384.1:c.-159_-155delinsGGCAA	XP_024308152.1:n.-159_-155delinsGGCAA
NM_001110792.2:c.157_161delinsGGCAA MANE Select	NP_001104262.1:p.Gly53=
NM_001316337.2:c.-159_-155delinsGGCAA	NP_001303266.1:n.-159_-155delinsGGCAA
NM_001369391.2:c.-159_-155delinsGGCAA	NP_001356320.1:n.-159_-155delinsGGCAA
NM_001369392.2:c.-159_-155delinsGGCAA	NP_001356321.1:n.-159_-155delinsGGCAA
NM_001369393.2:c.-159_-155delinsGGCAA	NP_001356322.1:n.-159_-155delinsGGCAA
NM_001369394.1:c.-159_-155delinsGGCAA	NP_001356323.1:n.-159_-155delinsGGCAA
NM_001369394.2:c.-159_-155delinsGGCAA	NP_001356323.1:n.-159_-155delinsGGCAA
NM_001386137.1:c.-440_-436delinsGGCAA	NP_001373066.1:n.-440_-436delinsGGCAA
NM_001386138.1:c.-440_-436delinsGGCAA	NP_001373067.1:n.-440_-436delinsGGCAA
NM_001386139.1:c.-440_-436delinsGGCAA	NP_001373068.1:n.-440_-436delinsGGCAA
NM_004992.4:c.121_125delinsGGCAA MANE Plus Clinical	NP_004983.1:p.Gly41=