Canonical Allele Identifier: CA2417979453
Gene: CDKL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18619993T= , CM000685.2:g.18619993T= GRCh38
NC_000023.10:g.18638113T= , CM000685.1:g.18638113T= GRCh37
NC_000023.9:g.18548034T= NCBI36
NG_008475.1:g.199389T=

Transcript Alleles

HGVS Amino-acid change
ENST00000623535.2:c.2376+27T= MANE Select ENSP00000485244.1:n.2376+27T=
ENST00000635828.1:c.2376+27T= ENSP00000490170.1:n.2376+27T=
ENST00000674046.1:c.2376+27T= ENSP00000501174.1:n.2376+27T=
ENST00000379989.6:c.2376+27T= ENSP00000369325.3:n.2376+27T=
ENST00000379996.7:c.2376+27T= ENSP00000369332.3:n.2376+27T=
ENST00000623535.1:c.2376+27T= ENSP00000485244.1:n.2376+27T=
NM_001037343.1:c.2376+27T= NP_001032420.1:n.2376+27T=
NM_003159.2:c.2376+27T= NP_003150.1:n.2376+27T=
XM_011545569.1:c.2325+27T= XP_011543871.1:n.2325+27T=
XM_011545570.1:c.2244+27T= XP_011543872.1:n.2244+27T=
XR_950484.1:n.2628+27T=
NM_001323289.1:c.2376+27T= NP_001310218.1:n.2376+27T=
NM_001323289.2:c.2376+27T= MANE Select NP_001310218.1:n.2376+27T=
NM_001037343.2:c.2376+27T= NP_001032420.1:n.2376+27T=
NM_003159.3:c.2376+27T= NP_003150.1:n.2376+27T=