Canonical Allele Identifier: CA2466570055
Gene: MECP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154030337_154030380delinsGGTTTGCTTTGCAATCCGCTCCGTGTAAAGTCAGCTAACTCTCT , CM000685.2:g.154030337_154030380delinsGGTTTGCTTTGCAATCCGCTCCGTGTAAAGTCAGCTAACTCTCT GRCh38
NC_000023.10:g.153295788_153295831delinsGGTTTGCTTTGCAATCCGCTCCGTGTAAAGTCAGCTAACTCTCT , CM000685.1:g.153295788_153295831delinsGGTTTGCTTTGCAATCCGCTCCGTGTAAAGTCAGCTAACTCTCT GRCh37
NC_000023.9:g.152948982_152949025delinsGGTTTGCTTTGCAATCCGCTCCGTGTAAAGTCAGCTAACTCTCT NCBI36
NG_007107.2:g.111748_111791delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC
NG_007107.3:g.111724_111767delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC

Transcript Alleles

HGVS Amino-acid change
ENST00000303391.11:c.1448_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC MANE Plus Clinical ENSP00000301948.6:n.[c.1448_*30delinsAGAG...
ENST00000453960.7:c.1484_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC MANE Select ENSP00000395535.2:n.[c.1484_*30delinsAGAG...
ENST00000303391.10:c.1448_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC ENSP00000301948.6:n.[c.1448_*30delinsAGAG...
ENST00000453960.6:c.1484_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC ENSP00000395535.2:n.[c.1484_*30delinsAGAG...
ENST00000619732.4:c.1448_1487delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC
ENST00000628176.2:c.*820_*863delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC ENSP00000486978.1:n.*820_*863delinsAGAGAG...
NM_001110792.1:c.1484_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC NP_001104262.1:n.[c.1484_*30delinsAGAGAGT...
NM_001316337.1:c.1169_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC NP_001303266.1:n.[c.1169_*30delinsAGAGAGT...
NM_004992.3:c.1448_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC NP_004983.1:n.[c.1448_*30delinsAGAGAGTTAG...
XM_005274681.3:c.1448_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC XP_005274738.1:n.[c.1448_*30delinsAGAGAGT...
XM_005274682.3:c.1169_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC XP_005274739.1:n.[c.1169_*30delinsAGAGAGT...
XM_005274683.3:c.1169_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC XP_005274740.1:n.[c.1169_*30delinsAGAGAGT...
XM_006724819.2:c.779_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC XP_006724882.1:n.[c.779_*30delinsAGAGAGTT...
XM_011531166.1:c.1169_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC XP_011529468.1:n.[c.1169_*30delinsAGAGAGT...
XM_006724819.3:c.779_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC XP_006724882.1:n.[c.779_*30delinsAGAGAGTT...
XM_011531166.2:c.1169_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC XP_011529468.1:n.[c.1169_*30delinsAGAGAGT...
XM_024452383.1:c.1169_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC XP_024308151.1:n.[c.1169_*30delinsAGAGAGT...
XM_024452384.1:c.1169_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC XP_024308152.1:n.[c.1169_*30delinsAGAGAGT...
NM_001110792.2:c.1484_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC MANE Select NP_001104262.1:n.[c.1484_*30delinsAGAGAGT...
NM_001316337.2:c.1169_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC NP_001303266.1:n.[c.1169_*30delinsAGAGAGT...
NM_001369391.2:c.1169_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC NP_001356320.1:n.[c.1169_*30delinsAGAGAGT...
NM_001369392.2:c.1169_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC NP_001356321.1:n.[c.1169_*30delinsAGAGAGT...
NM_001369393.2:c.1169_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC NP_001356322.1:n.[c.1169_*30delinsAGAGAGT...
NM_001369394.1:c.1169_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC NP_001356323.1:n.[c.1169_*30delinsAGAGAGT...
NM_001369394.2:c.1169_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC NP_001356323.1:n.[c.1169_*30delinsAGAGAGT...
NM_001386137.1:c.779_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC NP_001373066.1:n.[c.779_*30delinsAGAGAGTT...
NM_001386138.1:c.779_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC NP_001373067.1:n.[c.779_*30delinsAGAGAGTT...
NM_001386139.1:c.779_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC NP_001373068.1:n.[c.779_*30delinsAGAGAGTT...
NM_004992.4:c.1448_*30delinsAGAGAGTTAGCTGACTTTACACGGAGCGGATTGCAAAGCAAACC MANE Plus Clinical NP_004983.1:n.[c.1448_*30delinsAGAGAGTTAG...