Canonical Allele Identifier: CA415172971
Gene: MECP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154031204C>T , CM000685.2:g.154031204C>T GRCh38
NC_000023.10:g.153296655C>T , CM000685.1:g.153296655C>T GRCh37
NC_000023.9:g.152949849C>T NCBI36
NG_007107.2:g.110924G>A
NG_007107.3:g.110900G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.11:c.624G>A MANE Plus Clinical ENSP00000301948.6:p.Gln208=
ENST00000453960.7:c.660G>A MANE Select ENSP00000395535.2:p.Gln220=
ENST00000637917.1:c.65+192G>A
ENST00000303391.10:c.624G>A ENSP00000301948.6:p.Gln208=
ENST00000407218.5:c.551G>A ENSP00000384865.2:p.Arg184Lys
ENST00000453960.6:c.660G>A ENSP00000395535.2:p.Gln220=
ENST00000619732.4:c.624G>A ENSP00000480973.1:p.Gln208=
ENST00000622433.4:c.612G>A ENSP00000484470.1:p.Gln204=
ENST00000628176.2:c.515G>A ENSP00000486978.1:p.Arg172Lys
NM_001110792.1:c.660G>A NP_001104262.1:p.Gln220=
NM_001316337.1:c.345G>A NP_001303266.1:p.Gln115=
NM_004992.3:c.624G>A NP_004983.1:p.Gln208=
XM_005274681.3:c.624G>A XP_005274738.1:p.Gln208=
XM_005274682.3:c.345G>A XP_005274739.1:p.Gln115=
XM_005274683.3:c.345G>A XP_005274740.1:p.Gln115=
XM_006724819.2:c.-46G>A XP_006724882.1:n.-46G>A
XM_011531166.1:c.345G>A XP_011529468.1:p.Gln115=
XM_006724819.3:c.-46G>A XP_006724882.1:n.-46G>A
XM_011531166.2:c.345G>A XP_011529468.1:p.Gln115=
XM_024452383.1:c.345G>A XP_024308151.1:p.Gln115=
XM_024452384.1:c.345G>A XP_024308152.1:p.Gln115=
NM_001110792.2:c.660G>A MANE Select NP_001104262.1:p.Gln220=
NM_001316337.2:c.345G>A NP_001303266.1:p.Gln115=
NM_001369391.2:c.345G>A NP_001356320.1:p.Gln115=
NM_001369392.2:c.345G>A NP_001356321.1:p.Gln115=
NM_001369393.2:c.345G>A NP_001356322.1:p.Gln115=
NM_001369394.1:c.345G>A NP_001356323.1:p.Gln115=
NM_001369394.2:c.345G>A NP_001356323.1:p.Gln115=
NM_001386137.1:c.-46G>A NP_001373066.1:n.-46G>A
NM_001386138.1:c.-46G>A NP_001373067.1:n.-46G>A
NM_001386139.1:c.-46G>A NP_001373068.1:n.-46G>A
NM_004992.4:c.624G>A MANE Plus Clinical NP_004983.1:p.Gln208=