Canonical Allele Identifier: CA412363228

Gene: CDKL5

Linked Data

• ClinVar Variation Id: 1306443
• ClinVar RCV Id: RCV001760453
• dbSNP Id: rs2147161251
• MyVariant Identifiers: chrX:g.18622894G>T (hg19) ; chrX:g.18604774G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18604774G>T , CM000685.2:g.18604774G>T	GRCh38
NC_000023.10:g.18622894G>T , CM000685.1:g.18622894G>T	GRCh37
NC_000023.9:g.18532815G>T	NCBI36
NG_008475.1:g.184170G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.1850G>T MANE Select	ENSP00000485244.1:p.Arg617Leu
ENST00000635828.1:c.1850G>T	ENSP00000490170.1:p.Arg617Leu
ENST00000674046.1:c.1850G>T	ENSP00000501174.1:p.Arg617Leu
ENST00000379989.6:c.1850G>T	ENSP00000369325.3:p.Arg617Leu
ENST00000379996.7:c.1850G>T	ENSP00000369332.3:p.Arg617Leu
ENST00000463994.4:c.1850G>T	ENSP00000485184.1:p.Arg617Leu
ENST00000623535.1:c.1850G>T	ENSP00000485244.1:p.Arg617Leu
NM_001037343.1:c.1850G>T	NP_001032420.1:p.Arg617Leu
NM_003159.2:c.1850G>T	NP_003150.1:p.Arg617Leu
XM_011545569.1:c.1799G>T	XP_011543871.1:p.Arg600Leu
XM_011545570.1:c.1718G>T	XP_011543872.1:p.Arg573Leu
XR_950484.1:n.2102G>T
NM_001323289.1:c.1850G>T	NP_001310218.1:p.Arg617Leu
NM_001323289.2:c.1850G>T MANE Select	NP_001310218.1:p.Arg617Leu
NM_001037343.2:c.1850G>T	NP_001032420.1:p.Arg617Leu
NM_003159.3:c.1850G>T	NP_003150.1:p.Arg617Leu