Canonical Allele Identifier: CA412372333

Gene: RS1 CDKL5

Linked Data

• ClinVar Variation Id: 1444478
• ClinVar RCV Id: RCV001992367
• dbSNP Id: rs2147191395
• MyVariant Identifiers: chrX:g.18662731G>A (hg19) ; chrX:g.18644611G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18644611G>A , CM000685.2:g.18644611G>A	GRCh38
NC_000023.10:g.18662731G>A , CM000685.1:g.18662731G>A	GRCh37
NC_000023.9:g.18572652G>A	NCBI36
NG_008475.1:g.224007G>A
NG_008659.3:g.37838C>T , LRG_702:g.37838C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379984.4:c.341C>T (RS1) MANE Select	ENSP00000369320.3:p.Ser114Phe
ENST00000379984.3:c.341C>T (RS1)	ENSP00000369320.3:p.Ser114Phe
ENST00000379989.6:c.2714-1396G>A (CDKL5)	ENSP00000369325.3:n.2714-1396G>A
ENST00000379996.7:c.2714-1396G>A (CDKL5)	ENSP00000369332.3:n.2714-1396G>A
ENST00000476595.1:n.832C>T (RS1)
NM_000330.3:c.341C>T , LRG_702t1:c.341C>T (RS1)	NP_000321.1:p.Ser114Phe
NM_001037343.1:c.2714-1396G>A (CDKL5)	NP_001032420.1:n.2714-1396G>A
NM_003159.2:c.2714-1396G>A (CDKL5)	NP_003150.1:n.2714-1396G>A
XM_011545569.1:c.2786-1396G>A (CDKL5)	XP_011543871.1:n.2786-1396G>A
XM_011545570.1:c.2705-1396G>A (CDKL5)	XP_011543872.1:n.2705-1396G>A
XR_950484.1:n.3089-1396G>A (CDKL5)
NM_000330.4:c.341C>T (RS1) MANE Select	NP_000321.1:p.Ser114Phe
NM_001037343.2:c.2714-1396G>A (CDKL5)	NP_001032420.1:n.2714-1396G>A
NM_003159.3:c.2714-1396G>A (CDKL5)	NP_003150.1:n.2714-1396G>A