Canonical Allele Identifier: CA2417974428
Gene: CDKL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18604502T= , CM000685.2:g.18604502T= GRCh38
NC_000023.10:g.18622622T= , CM000685.1:g.18622622T= GRCh37
NC_000023.9:g.18532543T= NCBI36
NG_008475.1:g.183898T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000623535.2:c.1578T= MANE Select ENSP00000485244.1:p.Ser526=
ENST00000635828.1:c.1578T= ENSP00000490170.1:p.Ser526=
ENST00000674046.1:c.1578T= ENSP00000501174.1:p.Ser526=
ENST00000379989.6:c.1578T= ENSP00000369325.3:p.Ser526=
ENST00000379996.7:c.1578T= ENSP00000369332.3:p.Ser526=
ENST00000463994.4:c.1578T= ENSP00000485184.1:p.Ser526=
ENST00000623535.1:c.1578T= ENSP00000485244.1:p.Ser526=
NM_001037343.1:c.1578T= NP_001032420.1:p.Ser526=
NM_003159.2:c.1578T= NP_003150.1:p.Ser526=
XM_011545569.1:c.1527T= XP_011543871.1:p.Ser509=
XM_011545570.1:c.1446T= XP_011543872.1:p.Ser482=
XR_950484.1:n.1830T=
NM_001323289.1:c.1578T= NP_001310218.1:p.Ser526=
NM_001323289.2:c.1578T= MANE Select NP_001310218.1:p.Ser526=
NM_001037343.2:c.1578T= NP_001032420.1:p.Ser526=
NM_003159.3:c.1578T= NP_003150.1:p.Ser526=