Canonical Allele Identifier: CA2695105470

Gene: MECP2

Linked Data

• gnomAD v4: X-154097677-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097677C>T , CM000685.2:g.154097677C>T	GRCh38
NC_000023.10:g.153363134C>T , CM000685.1:g.153363134C>T	GRCh37
NC_000023.9:g.153016328C>T	NCBI36
NG_007107.2:g.44445G>A
NG_007107.3:g.44427G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000303391.11:c.-172G>A MANE Plus Clinical	ENSP00000301948.6:n.-172G>A
ENST00000453960.7:c.-12G>A MANE Select	ENSP00000395535.2:n.-12G>A
ENST00000303391.10:c.-172G>A	ENSP00000301948.6:n.-172G>A
ENST00000407218.5:c.-12G>A	ENSP00000384865.2:n.-12G>A
ENST00000453960.6:c.-12G>A	ENSP00000395535.2:n.-12G>A
ENST00000619732.4:c.-172G>A	ENSP00000480973.1:n.-172G>A
ENST00000627864.1:n.4G>A
ENST00000628176.2:c.-172G>A	ENSP00000486978.1:n.-172G>A
ENST00000631210.1:n.305+7104G>A
NM_001110792.1:c.-12G>A	NP_001104262.1:n.-12G>A
NM_001316337.1:c.-619G>A	NP_001303266.1:n.-619G>A
NM_004992.3:c.-172G>A	NP_004983.1:n.-172G>A
XM_005274682.3:c.-563G>A	XP_005274739.1:n.-563G>A
NM_001110792.2:c.-12G>A MANE Select	NP_001104262.1:n.-12G>A
NM_001316337.2:c.-619G>A	NP_001303266.1:n.-619G>A
NM_001369391.2:c.-914G>A	NP_001356320.1:n.-914G>A
NM_001369392.2:c.-563G>A	NP_001356321.1:n.-563G>A
NM_001369393.2:c.-439G>A	NP_001356322.1:n.-439G>A
NM_001386137.1:c.-844G>A	NP_001373066.1:n.-844G>A
NM_001386138.1:c.-732G>A	NP_001373067.1:n.-732G>A
NM_001386139.1:c.-608G>A	NP_001373068.1:n.-608G>A
NM_004992.4:c.-172G>A MANE Plus Clinical	NP_004983.1:n.-172G>A