Canonical Allele Identifier: CA2580100385
Gene: CDKL5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2105592
ClinVar RCV Id: RCV003023529

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18579937_18579950del , CM000685.2:g.18579937_18579950del GRCh38
NC_000023.10:g.18598057_18598070del , CM000685.1:g.18598057_18598070del GRCh37
NC_000023.9:g.18507978_18507991del NCBI36
NG_008475.1:g.159333_159346del

Transcript Alleles

HGVS Amino-acid Change
ENST00000623535.2:c.372_385del MANE Select ENSP00000485244.1:p.His124GlnfsTer2
ENST00000635828.1:c.372_385del ENSP00000490170.1:p.His124GlnfsTer2
ENST00000637881.1:c.372_385del ENSP00000489879.1:p.His124GlnfsTer2
ENST00000674046.1:c.372_385del ENSP00000501174.1:p.His124GlnfsTer2
ENST00000379989.6:c.372_385del ENSP00000369325.3:p.His124GlnfsTer2
ENST00000379996.7:c.372_385del ENSP00000369332.3:p.His124GlnfsTer2
ENST00000463994.4:c.372_385del ENSP00000485184.1:p.His124GlnfsTer2
ENST00000623535.1:c.372_385del ENSP00000485244.1:p.His124GlnfsTer2
NM_001037343.1:c.372_385del NP_001032420.1:p.His124GlnfsTer2
NM_003159.2:c.372_385del NP_003150.1:p.His124GlnfsTer2
XM_011545569.1:c.372_385del XP_011543871.1:p.His124GlnfsTer2
XM_011545570.1:c.240_253del XP_011543872.1:p.His80GlnfsTer2
XR_950484.1:n.624_637del
NM_001323289.1:c.372_385del NP_001310218.1:p.His124GlnfsTer2
NM_001323289.2:c.372_385del MANE Select NP_001310218.1:p.His124GlnfsTer2
NM_001037343.2:c.372_385del NP_001032420.1:p.His124GlnfsTer2
NM_003159.3:c.372_385del NP_003150.1:p.His124GlnfsTer2