Canonical Allele Identifier: CA226752

Gene: RS1 CDKL5

Linked Data

• ClinVar Variation Id: 98970
• ClinVar RCV Id: RCV000085311
• dbSNP Id: rs61753166
• MyVariant Identifiers: chrX:g.18662583C>T (hg19) ; chrX:g.18644463C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18644463C>T , CM000685.2:g.18644463C>T	GRCh38
NC_000023.10:g.18662583C>T , CM000685.1:g.18662583C>T	GRCh37
NC_000023.9:g.18572504C>T	NCBI36
NG_008475.1:g.223859C>T
NG_008659.3:g.37986G>A , LRG_702:g.37986G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000379984.4:c.489G>A (RS1) MANE Select	ENSP00000369320.3:p.Trp163Ter
ENST00000379984.3:c.489G>A (RS1)	ENSP00000369320.3:p.Trp163Ter
ENST00000379989.6:c.2714-1544C>T (CDKL5)	ENSP00000369325.3:n.2714-1544C>T
ENST00000379996.7:c.2714-1544C>T (CDKL5)	ENSP00000369332.3:n.2714-1544C>T
ENST00000476595.1:n.980G>A (RS1)
NM_000330.3:c.489G>A , LRG_702t1:c.489G>A (RS1)	NP_000321.1:p.Trp163Ter
NM_001037343.1:c.2714-1544C>T (CDKL5)	NP_001032420.1:n.2714-1544C>T
NM_003159.2:c.2714-1544C>T (CDKL5)	NP_003150.1:n.2714-1544C>T
XM_011545569.1:c.2786-1544C>T (CDKL5)	XP_011543871.1:n.2786-1544C>T
XM_011545570.1:c.2705-1544C>T (CDKL5)	XP_011543872.1:n.2705-1544C>T
XR_950484.1:n.3089-1544C>T (CDKL5)
NM_000330.4:c.489G>A (RS1) MANE Select	NP_000321.1:p.Trp163Ter
NM_001037343.2:c.2714-1544C>T (CDKL5)	NP_001032420.1:n.2714-1544C>T
NM_003159.3:c.2714-1544C>T (CDKL5)	NP_003150.1:n.2714-1544C>T