Canonical Allele Identifier: CA2695105550

Gene: MECP2

Linked Data

• gnomAD v4: X-154097724-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097724G>C , CM000685.2:g.154097724G>C	GRCh38
NC_000023.10:g.153363181G>C , CM000685.1:g.153363181G>C	GRCh37
NC_000023.9:g.153016375G>C	NCBI36
NG_007107.2:g.44398C>G
NG_007107.3:g.44380C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303391.10:c.-219C>G	ENSP00000301948.6:n.-219C>G
ENST00000453960.6:c.-59C>G	ENSP00000395535.2:n.-59C>G
ENST00000619732.4:c.-219C>G	ENSP00000480973.1:n.-219C>G
ENST00000628176.2:c.-219C>G	ENSP00000486978.1:n.-219C>G
ENST00000631210.1:n.305+7057C>G
NM_001110792.1:c.-59C>G	NP_001104262.1:n.-59C>G
NM_001316337.1:c.-666C>G	NP_001303266.1:n.-666C>G
NM_004992.3:c.-219C>G	NP_004983.1:n.-219C>G