Canonical Allele Identifier: CA2466570254
Gene: MECP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154030600_154030686delinsTGCTCAAGTCCTGGGGCTCAGGGGGGCTGGTGGGGTCCTCGGAGCTCTCGGGCTCAGGTGGAGGTGGGGGCAGGGGTGGGAGCAGTG , CM000685.2:g.154030600_154030686delinsTGCTCAAGTCCTGGGGCTCAGGGGGGCTGGTGGGGTCCTCGGAGCTCTCGGGCTCAGGTGGAGGTGGGGGCAGGGGTGGGAGCAGTG GRCh38
NC_000023.10:g.153296051_153296137delinsTGCTCAAGTCCTGGGGCTCAGGGGGGCTGGTGGGGTCCTCGGAGCTCTCGGGCTCAGGTGGAGGTGGGGGCAGGGGTGGGAGCAGTG , CM000685.1:g.153296051_153296137delinsTGCTCAAGTCCTGGGGCTCAGGGGGGCTGGTGGGGTCCTCGGAGCTCTCGGGCTCAGGTGGAGGTGGGGGCAGGGGTGGGAGCAGTG GRCh37
NC_000023.9:g.152949245_152949331delinsTGCTCAAGTCCTGGGGCTCAGGGGGGCTGGTGGGGTCCTCGGAGCTCTCGGGCTCAGGTGGAGGTGGGGGCAGGGGTGGGAGCAGTG NCBI36
NG_007107.2:g.111442_111528delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA
NG_007107.3:g.111418_111504delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA

Transcript Alleles

HGVS Amino-acid change
ENST00000303391.11:c.1142_1228delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA MANE Plus Clinical ENSP00000301948.6:p.Pro381=
ENST00000453960.7:c.1178_1264delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA MANE Select ENSP00000395535.2:p.Pro393=
ENST00000303391.10:c.1142_1228delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA ENSP00000301948.6:p.Pro381=
ENST00000453960.6:c.1178_1264delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA ENSP00000395535.2:p.Pro393=
ENST00000619732.4:c.1142_1228delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA ENSP00000480973.1:p.Pro381=
ENST00000628176.2:c.*514_*600delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA ENSP00000486978.1:n.*514_*600delinsCACTGCTCCCACCCCTGCCCCCACCT...
NM_001110792.1:c.1178_1264delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA NP_001104262.1:p.Pro393=
NM_001316337.1:c.863_949delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA NP_001303266.1:p.Pro288=
NM_004992.3:c.1142_1228delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA NP_004983.1:p.Pro381=
XM_005274681.3:c.1142_1228delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA XP_005274738.1:p.Pro381=
XM_005274682.3:c.863_949delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA XP_005274739.1:p.Pro288=
XM_005274683.3:c.863_949delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA XP_005274740.1:p.Pro288=
XM_006724819.2:c.473_559delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA XP_006724882.1:p.Pro158=
XM_011531166.1:c.863_949delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA XP_011529468.1:p.Pro288=
XM_006724819.3:c.473_559delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA XP_006724882.1:p.Pro158=
XM_011531166.2:c.863_949delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA XP_011529468.1:p.Pro288=
XM_024452383.1:c.863_949delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA XP_024308151.1:p.Pro288=
XM_024452384.1:c.863_949delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA XP_024308152.1:p.Pro288=
NM_001110792.2:c.1178_1264delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA MANE Select NP_001104262.1:p.Pro393=
NM_001316337.2:c.863_949delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA NP_001303266.1:p.Pro288=
NM_001369391.2:c.863_949delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA NP_001356320.1:p.Pro288=
NM_001369392.2:c.863_949delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA NP_001356321.1:p.Pro288=
NM_001369393.2:c.863_949delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA NP_001356322.1:p.Pro288=
NM_001369394.1:c.863_949delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA NP_001356323.1:p.Pro288=
NM_001369394.2:c.863_949delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA NP_001356323.1:p.Pro288=
NM_001386137.1:c.473_559delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA NP_001373066.1:p.Pro158=
NM_001386138.1:c.473_559delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA NP_001373067.1:p.Pro158=
NM_001386139.1:c.473_559delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA NP_001373068.1:p.Pro158=
NM_004992.4:c.1142_1228delinsCACTGCTCCCACCCCTGCCCCCACCTCCACCTGAGCCCGAGAGCTCCGAGGACCCCACCAGCCCCCCTGAGCCCCAGGACTTGAGCA MANE Plus Clinical NP_004983.1:p.Pro381=