Canonical Allele Identifier: CA2695100357
Gene: MECP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154032482_154032490dup , CM000685.2:g.154032482_154032490dup GRCh38
NC_000023.10:g.153297933_153297941dup , CM000685.1:g.153297933_153297941dup GRCh37
NC_000023.9:g.152951127_152951135dup NCBI36
NG_007107.2:g.109646_109654dup
NG_007107.3:g.109622_109630dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.102_110dup MANE Plus Clinical ENSP00000301948.6:p.Lys36_Glu37insAspLysLys
ENST00000453960.7:c.138_146dup MANE Select ENSP00000395535.2:p.Lys48_Glu49insAspLysLys
ENST00000611468.2:n.350_358dup
ENST00000630151.2:c.102_110dup ENSP00000486089.1:p.Lys36_Glu37insAspLysLys
ENST00000676382.1:n.295_303dup
ENST00000303391.10:c.102_110dup ENSP00000301948.6:p.Lys36_Glu37insAspLysLys
ENST00000369957.5:c.*156_*164dup ENSP00000358973.4:n.*156_*164dup
ENST00000407218.5:c.138_146dup ENSP00000384865.2:p.Lys48_Glu49insAspLysLys
ENST00000415944.3:c.102_110dup ENSP00000416267.1:p.Lys36_Glu37insAspLysLys
ENST00000453960.6:c.138_146dup ENSP00000395535.2:p.Lys48_Glu49insAspLysLys
ENST00000460227.4:n.1251_1259dup
ENST00000463644.5:n.1041_1049dup
ENST00000481807.3:n.388_396dup
ENST00000486506.5:n.2450_2458dup
ENST00000488293.4:n.1151_1159dup
ENST00000496908.5:n.233_241dup
ENST00000611468.1:c.90_98dup ENSP00000479736.1:p.Lys32_Glu33insAspLysLys
ENST00000619732.4:c.102_110dup ENSP00000480973.1:p.Lys36_Glu37insAspLysLys
ENST00000622433.4:c.90_98dup ENSP00000484470.1:p.Lys32_Glu33insAspLysLys
ENST00000625300.1:n.327_335dup
ENST00000626422.2:n.812_820dup
ENST00000628176.2:c.102_110dup ENSP00000486978.1:p.Lys36_Glu37insAspLysLys
ENST00000630151.1:c.102_110dup ENSP00000486089.1:p.Lys36_Glu37insAspLysLys
ENST00000631210.1:n.381_389dup
NM_001110792.1:c.138_146dup NP_001104262.1:p.Lys48_Glu49insAspLysLys
NM_001316337.1:c.-178_-170dup NP_001303266.1:n.-178_-170dup
NM_004992.3:c.102_110dup NP_004983.1:p.Lys36_Glu37insAspLysLys
XM_005274681.3:c.102_110dup XP_005274738.1:p.Lys36_Glu37insAspLysLys
XM_005274682.3:c.-178_-170dup XP_005274739.1:n.-178_-170dup
XM_005274683.3:c.-178_-170dup XP_005274740.1:n.-178_-170dup
XM_011531166.1:c.-178_-170dup XP_011529468.1:n.-178_-170dup
XM_006724819.3:c.-459_-451dup XP_006724882.1:n.-459_-451dup
XM_011531166.2:c.-178_-170dup XP_011529468.1:n.-178_-170dup
XM_024452383.1:c.-178_-170dup XP_024308151.1:n.-178_-170dup
XM_024452384.1:c.-178_-170dup XP_024308152.1:n.-178_-170dup
NM_001110792.2:c.138_146dup MANE Select NP_001104262.1:p.Lys48_Glu49insAspLysLys
NM_001316337.2:c.-178_-170dup NP_001303266.1:n.-178_-170dup
NM_001369391.2:c.-178_-170dup NP_001356320.1:n.-178_-170dup
NM_001369392.2:c.-178_-170dup NP_001356321.1:n.-178_-170dup
NM_001369393.2:c.-178_-170dup NP_001356322.1:n.-178_-170dup
NM_001369394.1:c.-178_-170dup NP_001356323.1:n.-178_-170dup
NM_001369394.2:c.-178_-170dup NP_001356323.1:n.-178_-170dup
NM_001386137.1:c.-459_-451dup NP_001373066.1:n.-459_-451dup
NM_001386138.1:c.-459_-451dup NP_001373067.1:n.-459_-451dup
NM_001386139.1:c.-459_-451dup NP_001373068.1:n.-459_-451dup
NM_004992.4:c.102_110dup MANE Plus Clinical NP_004983.1:p.Lys36_Glu37insAspLysLys