Canonical Allele Identifier: CA515474216

Gene: RS1 CDKL5

Linked Data

• ClinVar Variation Id: 1126621
• ClinVar RCV Id: RCV001458773
• dbSNP Id: rs1927704453
• gnomAD v4: X-18644598-G-A
• MyVariant Identifiers: chrX:g.18662718G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18644598G>A , CM000685.2:g.18644598G>A	GRCh38
NC_000023.10:g.18662718G>A , CM000685.1:g.18662718G>A	GRCh37
NC_000023.9:g.18572639G>A	NCBI36
NG_008475.1:g.223994G>A
NG_008659.3:g.37851C>T , LRG_702:g.37851C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379984.4:c.354C>T (RS1) MANE Select	ENSP00000369320.3:p.Asp118=
ENST00000379984.3:c.354C>T (RS1)	ENSP00000369320.3:p.Asp118=
ENST00000379989.6:c.2714-1409G>A (CDKL5)	ENSP00000369325.3:n.2714-1409G>A
ENST00000379996.7:c.2714-1409G>A (CDKL5)	ENSP00000369332.3:n.2714-1409G>A
ENST00000476595.1:n.845C>T (RS1)
NM_000330.3:c.354C>T , LRG_702t1:c.354C>T (RS1)	NP_000321.1:p.Asp118=
NM_001037343.1:c.2714-1409G>A (CDKL5)	NP_001032420.1:n.2714-1409G>A
NM_003159.2:c.2714-1409G>A (CDKL5)	NP_003150.1:n.2714-1409G>A
XM_011545569.1:c.2786-1409G>A (CDKL5)	XP_011543871.1:n.2786-1409G>A
XM_011545570.1:c.2705-1409G>A (CDKL5)	XP_011543872.1:n.2705-1409G>A
XR_950484.1:n.3089-1409G>A (CDKL5)
NM_000330.4:c.354C>T (RS1) MANE Select	NP_000321.1:p.Asp118=
NM_001037343.2:c.2714-1409G>A (CDKL5)	NP_001032420.1:n.2714-1409G>A
NM_003159.3:c.2714-1409G>A (CDKL5)	NP_003150.1:n.2714-1409G>A