Canonical Allele Identifier: CA2417982242
Gene: CDKL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18628652C= , CM000685.2:g.18628652C= GRCh38
NC_000023.10:g.18646772C= , CM000685.1:g.18646772C= GRCh37
NC_000023.9:g.18556693C= NCBI36
NG_008475.1:g.208048C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000623535.2:c.2778C= MANE Select ENSP00000485244.1:p.Tyr926=
ENST00000674046.1:c.2901C= ENSP00000501174.1:p.Tyr967=
ENST00000379989.6:c.2713+65C= ENSP00000369325.3:n.2713+65C=
ENST00000379996.7:c.2713+65C= ENSP00000369332.3:n.2713+65C=
ENST00000623535.1:c.2778C= ENSP00000485244.1:p.Tyr926=
NM_001037343.1:c.2713+65C= NP_001032420.1:n.2713+65C=
NM_003159.2:c.2713+65C= NP_003150.1:n.2713+65C=
XM_011545569.1:c.2785+65C= XP_011543871.1:n.2785+65C=
XM_011545570.1:c.2704+65C= XP_011543872.1:n.2704+65C=
XR_950484.1:n.3088+65C=
NM_001323289.1:c.2778C= NP_001310218.1:p.Tyr926=
NM_001323289.2:c.2778C= MANE Select NP_001310218.1:p.Tyr926=
NM_001037343.2:c.2713+65C= NP_001032420.1:n.2713+65C=
NM_003159.3:c.2713+65C= NP_003150.1:n.2713+65C=