Canonical Allele Identifier: CA2573159392
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1354117
ClinVar RCV Id: RCV001874032
dbSNP Id: rs2148667088

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154032477_154032481del , CM000685.2:g.154032477_154032481del GRCh38
NC_000023.10:g.153297928_153297932del , CM000685.1:g.153297928_153297932del GRCh37
NC_000023.9:g.152951122_152951126del NCBI36
NG_007107.2:g.109648_109652del
NG_007107.3:g.109624_109628del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.104_108del MANE Plus Clinical ENSP00000301948.6:p.Lys35ArgfsTer8
ENST00000453960.7:c.140_144del MANE Select ENSP00000395535.2:p.Lys47ArgfsTer8
ENST00000611468.2:n.352_356del
ENST00000630151.2:c.104_108del ENSP00000486089.1:p.Lys35ArgfsTer?
ENST00000637533.1:n.135_139del
ENST00000676382.1:n.297_301del
ENST00000303391.10:c.104_108del ENSP00000301948.6:p.Lys35ArgfsTer8
ENST00000369957.5:c.*158_*162del ENSP00000358973.4:n.*158_*162del
ENST00000407218.5:c.140_144del ENSP00000384865.2:p.Lys47ArgfsTer8
ENST00000415944.3:c.104_108del ENSP00000416267.1:p.Lys35ArgfsTer8
ENST00000453960.6:c.140_144del ENSP00000395535.2:p.Lys47ArgfsTer8
ENST00000460227.4:n.1253_1257del
ENST00000463644.5:n.1043_1047del
ENST00000481807.3:n.390_394del
ENST00000486506.5:n.2452_2456del
ENST00000488293.4:n.1153_1157del
ENST00000496908.5:n.235_239del
ENST00000611468.1:c.92_96del ENSP00000479736.1:p.Lys31ArgfsTer8
ENST00000619732.4:c.104_108del ENSP00000480973.1:p.Lys35ArgfsTer8
ENST00000622433.4:c.92_96del ENSP00000484470.1:p.Lys31ArgfsTer8
ENST00000625300.1:n.329_333del
ENST00000626422.2:n.814_818del
ENST00000628176.2:c.104_108del ENSP00000486978.1:p.Lys35ArgfsTer8
ENST00000630151.1:c.104_108del ENSP00000486089.1:p.Lys35ArgfsTer?
ENST00000631210.1:n.383_387del
NM_001110792.1:c.140_144del NP_001104262.1:p.Lys47ArgfsTer8
NM_001316337.1:c.-176_-172del NP_001303266.1:n.-176_-172del
NM_004992.3:c.104_108del NP_004983.1:p.Lys35ArgfsTer8
XM_005274681.3:c.104_108del XP_005274738.1:p.Lys35ArgfsTer8
XM_005274682.3:c.-176_-172del XP_005274739.1:n.-176_-172del
XM_005274683.3:c.-176_-172del XP_005274740.1:n.-176_-172del
XM_011531166.1:c.-176_-172del XP_011529468.1:n.-176_-172del
XM_006724819.3:c.-457_-453del XP_006724882.1:n.-457_-453del
XM_011531166.2:c.-176_-172del XP_011529468.1:n.-176_-172del
XM_024452383.1:c.-176_-172del XP_024308151.1:n.-176_-172del
XM_024452384.1:c.-176_-172del XP_024308152.1:n.-176_-172del
NM_001110792.2:c.140_144del MANE Select NP_001104262.1:p.Lys47ArgfsTer8
NM_001316337.2:c.-176_-172del NP_001303266.1:n.-176_-172del
NM_001369391.2:c.-176_-172del NP_001356320.1:n.-176_-172del
NM_001369392.2:c.-176_-172del NP_001356321.1:n.-176_-172del
NM_001369393.2:c.-176_-172del NP_001356322.1:n.-176_-172del
NM_001369394.1:c.-176_-172del NP_001356323.1:n.-176_-172del
NM_001369394.2:c.-176_-172del NP_001356323.1:n.-176_-172del
NM_001386137.1:c.-457_-453del NP_001373066.1:n.-457_-453del
NM_001386138.1:c.-457_-453del NP_001373067.1:n.-457_-453del
NM_001386139.1:c.-457_-453del NP_001373068.1:n.-457_-453del
NM_004992.4:c.104_108del MANE Plus Clinical NP_004983.1:p.Lys35ArgfsTer8