Canonical Allele Identifier: CA16616641

Gene: CDKL5

Linked Data

• ClinVar Variation Id: 408121
• ClinVar RCV Id: RCV000474894
• dbSNP Id: rs1060501859
• MyVariant Identifiers: chrX:g.18616580A>G (hg19) ; chrX:g.18598460A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18598460A>G , CM000685.2:g.18598460A>G	GRCh38
NC_000023.10:g.18616580A>G , CM000685.1:g.18616580A>G	GRCh37
NC_000023.9:g.18526501A>G	NCBI36
NG_008475.1:g.177856A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.826-2A>G MANE Select	ENSP00000485244.1:n.826-2A>G
ENST00000635828.1:c.826-2A>G	ENSP00000490170.1:n.826-2A>G
ENST00000637881.1:c.826-2A>G	ENSP00000489879.1:n.826-2A>G
ENST00000674046.1:c.826-2A>G	ENSP00000501174.1:n.826-2A>G
ENST00000379989.6:c.826-2A>G	ENSP00000369325.3:n.826-2A>G
ENST00000379996.7:c.826-2A>G	ENSP00000369332.3:n.826-2A>G
ENST00000463994.4:c.826-2A>G	ENSP00000485184.1:n.826-2A>G
ENST00000623535.1:c.826-2A>G	ENSP00000485244.1:n.826-2A>G
NM_001037343.1:c.826-2A>G	NP_001032420.1:n.826-2A>G
NM_003159.2:c.826-2A>G	NP_003150.1:n.826-2A>G
XM_011545569.1:c.826-2A>G	XP_011543871.1:n.826-2A>G
XM_011545570.1:c.694-2A>G	XP_011543872.1:n.694-2A>G
XR_950484.1:n.1078-2A>G
NM_001323289.1:c.826-2A>G	NP_001310218.1:n.826-2A>G
NM_001323289.2:c.826-2A>G MANE Select	NP_001310218.1:n.826-2A>G
NM_001037343.2:c.826-2A>G	NP_001032420.1:n.826-2A>G
NM_003159.3:c.826-2A>G	NP_003150.1:n.826-2A>G