Canonical Allele Identifier: CA10360594

Gene: RS1 CDKL5

Linked Data

• ClinVar Variation Id: 3035108
• ClinVar RCV Id: RCV003909596
• dbSNP Id: rs756606916
• ExAC: X:18660122 C / A
• gnomAD v2: X-18660122-C-A
• gnomAD v3: X-18642002-C-A
• gnomAD v4: X-18642002-C-A
• MyVariant Identifiers: chrX:g.18660122C>A (hg19) ; chrX:g.18642002C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18642002C>A , CM000685.2:g.18642002C>A	GRCh38
NC_000023.10:g.18660122C>A , CM000685.1:g.18660122C>A	GRCh37
NC_000023.9:g.18570043C>A	NCBI36
NG_008475.1:g.221398C>A
NG_008659.3:g.40447G>T , LRG_702:g.40447G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000379984.4:c.*2G>T (RS1) MANE Select	ENSP00000369320.3:n.*2G>T
ENST00000379984.3:c.*2G>T (RS1)	ENSP00000369320.3:n.*2G>T
ENST00000379989.6:c.2714-4005C>A (CDKL5)	ENSP00000369325.3:n.2714-4005C>A
ENST00000379996.7:c.2714-4005C>A (CDKL5)	ENSP00000369332.3:n.2714-4005C>A
ENST00000476595.1:n.1168G>T (RS1)
NM_000330.3:c.*2G>T , LRG_702t1:c.*2G>T (RS1)	NP_000321.1:n.*2G>T
NM_001037343.1:c.2714-4005C>A (CDKL5)	NP_001032420.1:n.2714-4005C>A
NM_003159.2:c.2714-4005C>A (CDKL5)	NP_003150.1:n.2714-4005C>A
XM_011545569.1:c.2786-4005C>A (CDKL5)	XP_011543871.1:n.2786-4005C>A
XM_011545570.1:c.2705-4005C>A (CDKL5)	XP_011543872.1:n.2705-4005C>A
XR_950484.1:n.3089-4005C>A (CDKL5)
NM_000330.4:c.*2G>T (RS1) MANE Select	NP_000321.1:n.*2G>T
NM_001037343.2:c.2714-4005C>A (CDKL5)	NP_001032420.1:n.2714-4005C>A
NM_003159.3:c.2714-4005C>A (CDKL5)	NP_003150.1:n.2714-4005C>A