Canonical Allele Identifier: CA412363064

Gene: CDKL5

Linked Data

• ClinVar Variation Id: 2941715
• ClinVar RCV Id: RCV003802737
• MyVariant Identifiers: chrX:g.18637987G>A (hg19) ; chrX:g.18619867G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18619867G>A , CM000685.2:g.18619867G>A	GRCh38
NC_000023.10:g.18637987G>A , CM000685.1:g.18637987G>A	GRCh37
NC_000023.9:g.18547908G>A	NCBI36
NG_008475.1:g.199263G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.2277G>A MANE Select	ENSP00000485244.1:p.Trp759Ter
ENST00000635828.1:c.2277G>A	ENSP00000490170.1:p.Trp759Ter
ENST00000674046.1:c.2277G>A	ENSP00000501174.1:p.Trp759Ter
ENST00000379989.6:c.2277G>A	ENSP00000369325.3:p.Trp759Ter
ENST00000379996.7:c.2277G>A	ENSP00000369332.3:p.Trp759Ter
ENST00000463994.4:c.2277G>A	ENSP00000485184.1:p.Trp759Ter
ENST00000623535.1:c.2277G>A	ENSP00000485244.1:p.Trp759Ter
NM_001037343.1:c.2277G>A	NP_001032420.1:p.Trp759Ter
NM_003159.2:c.2277G>A	NP_003150.1:p.Trp759Ter
XM_011545569.1:c.2226G>A	XP_011543871.1:p.Trp742Ter
XM_011545570.1:c.2145G>A	XP_011543872.1:p.Trp715Ter
XR_950484.1:n.2529G>A
NM_001323289.1:c.2277G>A	NP_001310218.1:p.Trp759Ter
NM_001323289.2:c.2277G>A MANE Select	NP_001310218.1:p.Trp759Ter
NM_001037343.2:c.2277G>A	NP_001032420.1:p.Trp759Ter
NM_003159.3:c.2277G>A	NP_003150.1:p.Trp759Ter