Canonical Allele Identifier: CA327011724

Gene: RS1 CDKL5

Linked Data

• ClinVar Variation Id: 1461348
• ClinVar RCV Id: RCV001983312
• dbSNP Id: rs1005590954
• gnomAD v2: X-18662761-C-T
• gnomAD v3: X-18644641-C-T
• gnomAD v4: X-18644641-C-T
• COSMIC: COSN168719
• MyVariant Identifiers: chrX:g.18662761C>T (hg19) ; chrX:g.18644641C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18644641C>T , CM000685.2:g.18644641C>T	GRCh38
NC_000023.10:g.18662761C>T , CM000685.1:g.18662761C>T	GRCh37
NC_000023.9:g.18572682C>T	NCBI36
NG_008475.1:g.224037C>T
NG_008659.3:g.37808G>A , LRG_702:g.37808G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379984.4:c.327-16G>A (RS1) MANE Select	ENSP00000369320.3:n.327-16G>A
ENST00000379984.3:c.327-16G>A (RS1)	ENSP00000369320.3:n.327-16G>A
ENST00000379989.6:c.2714-1366C>T (CDKL5)	ENSP00000369325.3:n.2714-1366C>T
ENST00000379996.7:c.2714-1366C>T (CDKL5)	ENSP00000369332.3:n.2714-1366C>T
ENST00000476595.1:n.818-16G>A (RS1)
NM_000330.3:c.327-16G>A , LRG_702t1:c.327-16G>A (RS1)	NP_000321.1:n.327-16G>A
NM_001037343.1:c.2714-1366C>T (CDKL5)	NP_001032420.1:n.2714-1366C>T
NM_003159.2:c.2714-1366C>T (CDKL5)	NP_003150.1:n.2714-1366C>T
XM_011545569.1:c.2786-1366C>T (CDKL5)	XP_011543871.1:n.2786-1366C>T
XM_011545570.1:c.2705-1366C>T (CDKL5)	XP_011543872.1:n.2705-1366C>T
XR_950484.1:n.3089-1366C>T (CDKL5)
NM_000330.4:c.327-16G>A (RS1) MANE Select	NP_000321.1:n.327-16G>A
NM_001037343.2:c.2714-1366C>T (CDKL5)	NP_001032420.1:n.2714-1366C>T
NM_003159.3:c.2714-1366C>T (CDKL5)	NP_003150.1:n.2714-1366C>T