Canonical Allele Identifier: CA2466568660
Gene: MECP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154028011A= , CM000685.2:g.154028011A= GRCh38
NC_000023.10:g.153293462A= , CM000685.1:g.153293462A= GRCh37
NC_000023.9:g.152946656A= NCBI36
NG_007107.2:g.114117T=
NG_007107.3:g.114093T=

Transcript Alleles

HGVS Amino-acid change
ENST00000303391.11:c.*2356T= MANE Plus Clinical ENSP00000301948.6:n.*2356T=
ENST00000453960.7:c.*2356T= MANE Select ENSP00000395535.2:n.*2356T=
ENST00000303391.10:c.*2356T= ENSP00000301948.6:n.*2356T=
ENST00000619732.4:c.*2283T= ENSP00000480973.1:n.*2283T=
NM_004992.3:c.*2356T= NP_004983.1:n.*2356T=
XM_006724819.3:c.*2356T= XP_006724882.1:n.*2356T=
XM_011531166.2:c.*2356T= XP_011529468.1:n.*2356T=
XM_024452383.1:c.*2356T= XP_024308151.1:n.*2356T=
XM_024452384.1:c.*2356T= XP_024308152.1:n.*2356T=
NM_001110792.2:c.*2356T= MANE Select NP_001104262.1:n.*2356T=
NM_001316337.2:c.*2356T= NP_001303266.1:n.*2356T=
NM_001369391.2:c.*2356T= NP_001356320.1:n.*2356T=
NM_001369392.2:c.*2356T= NP_001356321.1:n.*2356T=
NM_001369393.2:c.*2356T= NP_001356322.1:n.*2356T=
NM_001369394.2:c.*2356T= NP_001356323.1:n.*2356T=
NM_001386137.1:c.*2356T= NP_001373066.1:n.*2356T=
NM_001386138.1:c.*2356T= NP_001373067.1:n.*2356T=
NM_001386139.1:c.*2356T= NP_001373068.1:n.*2356T=
NM_004992.4:c.*2356T= MANE Plus Clinical NP_004983.1:n.*2356T=