Canonical Allele Identifier: CA2417982233
Gene: CDKL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18628607G= , CM000685.2:g.18628607G= GRCh38
NC_000023.10:g.18646727G= , CM000685.1:g.18646727G= GRCh37
NC_000023.9:g.18556648G= NCBI36
NG_008475.1:g.208003G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000623535.2:c.2733G= MANE Select ENSP00000485244.1:p.Trp911=
ENST00000674046.1:c.2856G= ENSP00000501174.1:p.Trp952=
ENST00000379989.6:c.2713+20G= ENSP00000369325.3:n.2713+20G=
ENST00000379996.7:c.2713+20G= ENSP00000369332.3:n.2713+20G=
ENST00000623535.1:c.2733G= ENSP00000485244.1:p.Trp911=
NM_001037343.1:c.2713+20G= NP_001032420.1:n.2713+20G=
NM_003159.2:c.2713+20G= NP_003150.1:n.2713+20G=
XM_011545569.1:c.2785+20G= XP_011543871.1:n.2785+20G=
XM_011545570.1:c.2704+20G= XP_011543872.1:n.2704+20G=
XR_950484.1:n.3088+20G=
NM_001323289.1:c.2733G= NP_001310218.1:p.Trp911=
NM_001323289.2:c.2733G= MANE Select NP_001310218.1:p.Trp911=
NM_001037343.2:c.2713+20G= NP_001032420.1:n.2713+20G=
NM_003159.3:c.2713+20G= NP_003150.1:n.2713+20G=