Canonical Allele Identifier: CA645372671

Gene: CDKL5

Linked Data

• ClinVar Variation Id: 437405
• ClinVar RCV Id: RCV000500125
• dbSNP Id: rs1555954078
• MyVariant Identifiers: chrX:g.18638069_18638073del (hg19) ; chrX:g.18619949_18619953del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18619949_18619953del , CM000685.2:g.18619949_18619953del	GRCh38
NC_000023.10:g.18638069_18638073del , CM000685.1:g.18638069_18638073del	GRCh37
NC_000023.9:g.18547990_18547994del	NCBI36
NG_008475.1:g.199345_199349del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.2359_2363del MANE Select	ENSP00000485244.1:p.Lys787GlufsTer12
ENST00000635828.1:c.2359_2363del	ENSP00000490170.1:p.Lys787GlufsTer12
ENST00000674046.1:c.2359_2363del	ENSP00000501174.1:p.Lys787GlufsTer24
ENST00000379989.6:c.2359_2363del	ENSP00000369325.3:p.Lys787GlufsTer12
ENST00000379996.7:c.2359_2363del	ENSP00000369332.3:p.Lys787GlufsTer12
ENST00000623535.1:c.2359_2363del	ENSP00000485244.1:p.Lys787GlufsTer12
NM_001037343.1:c.2359_2363del	NP_001032420.1:p.Lys787GlufsTer12
NM_003159.2:c.2359_2363del	NP_003150.1:p.Lys787GlufsTer12
XM_011545569.1:c.2308_2312del	XP_011543871.1:p.Lys770GlufsTer24
XM_011545570.1:c.2227_2231del	XP_011543872.1:p.Lys743GlufsTer24
XR_950484.1:n.2611_2615del
NM_001323289.1:c.2359_2363del	NP_001310218.1:p.Lys787GlufsTer12
NM_001323289.2:c.2359_2363del MANE Select	NP_001310218.1:p.Lys787GlufsTer12
NM_001037343.2:c.2359_2363del	NP_001032420.1:p.Lys787GlufsTer12
NM_003159.3:c.2359_2363del	NP_003150.1:p.Lys787GlufsTer12