Canonical Allele Identifier: CA2579736490
Gene: MECP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154032146_154032157dup , CM000685.2:g.154032146_154032157dup GRCh38
NC_000023.10:g.153297597_153297608dup , CM000685.1:g.153297597_153297608dup GRCh37
NC_000023.9:g.152950791_152950802dup NCBI36
NG_007107.2:g.109972_109983dup
NG_007107.3:g.109948_109959dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.377+51_377+62dup MANE Plus Clinical ENSP00000301948.6:n.377+51_377+62dup
ENST00000453960.7:c.413+51_413+62dup MANE Select ENSP00000395535.2:n.413+51_413+62dup
ENST00000637917.1:c.10+51_10+62dup
ENST00000303391.10:c.377+51_377+62dup ENSP00000301948.6:n.377+51_377+62dup
ENST00000369957.5:c.*431+51_*431+62dup ENSP00000358973.4:n.*431+51_*431+62dup
ENST00000407218.5:c.413+51_413+62dup ENSP00000384865.2:n.413+51_413+62dup
ENST00000453960.6:c.413+51_413+62dup ENSP00000395535.2:n.413+51_413+62dup
ENST00000486506.5:n.2725+51_2725+62dup
ENST00000611468.1:c.365+51_365+62dup ENSP00000479736.1:n.365+51_365+62dup
ENST00000619732.4:c.377+51_377+62dup ENSP00000480973.1:n.377+51_377+62dup
ENST00000622433.4:c.365+51_365+62dup ENSP00000484470.1:n.365+51_365+62dup
ENST00000628176.2:c.377+51_377+62dup ENSP00000486978.1:n.377+51_377+62dup
NM_001110792.1:c.413+51_413+62dup NP_001104262.1:n.413+51_413+62dup
NM_001316337.1:c.98+51_98+62dup NP_001303266.1:n.98+51_98+62dup
NM_004992.3:c.377+51_377+62dup NP_004983.1:n.377+51_377+62dup
XM_005274681.3:c.377+51_377+62dup XP_005274738.1:n.377+51_377+62dup
XM_005274682.3:c.98+51_98+62dup XP_005274739.1:n.98+51_98+62dup
XM_005274683.3:c.98+51_98+62dup XP_005274740.1:n.98+51_98+62dup
XM_006724819.2:c.-184+51_-184+62dup XP_006724882.1:n.-184+51_-184+62dup
XM_011531166.1:c.98+51_98+62dup XP_011529468.1:n.98+51_98+62dup
XM_006724819.3:c.-184+51_-184+62dup XP_006724882.1:n.-184+51_-184+62dup
XM_011531166.2:c.98+51_98+62dup XP_011529468.1:n.98+51_98+62dup
XM_024452383.1:c.98+51_98+62dup XP_024308151.1:n.98+51_98+62dup
XM_024452384.1:c.98+51_98+62dup XP_024308152.1:n.98+51_98+62dup
NM_001110792.2:c.413+51_413+62dup MANE Select NP_001104262.1:n.413+51_413+62dup
NM_001316337.2:c.98+51_98+62dup NP_001303266.1:n.98+51_98+62dup
NM_001369391.2:c.98+51_98+62dup NP_001356320.1:n.98+51_98+62dup
NM_001369392.2:c.98+51_98+62dup NP_001356321.1:n.98+51_98+62dup
NM_001369393.2:c.98+51_98+62dup NP_001356322.1:n.98+51_98+62dup
NM_001369394.1:c.98+51_98+62dup NP_001356323.1:n.98+51_98+62dup
NM_001369394.2:c.98+51_98+62dup NP_001356323.1:n.98+51_98+62dup
NM_001386137.1:c.-184+51_-184+62dup NP_001373066.1:n.-184+51_-184+62dup
NM_001386138.1:c.-184+51_-184+62dup NP_001373067.1:n.-184+51_-184+62dup
NM_001386139.1:c.-184+51_-184+62dup NP_001373068.1:n.-184+51_-184+62dup
NM_004992.4:c.377+51_377+62dup MANE Plus Clinical NP_004983.1:n.377+51_377+62dup