Canonical Allele Identifier: CA412349760
Gene: CDKL5 HGNC NCBI

Linked Data

gnomAD v4: X-18579854-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18579854C>T , CM000685.2:g.18579854C>T GRCh38
NC_000023.10:g.18597974C>T , CM000685.1:g.18597974C>T GRCh37
NC_000023.9:g.18507895C>T NCBI36
NG_008475.1:g.159250C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000623535.2:c.289C>T MANE Select ENSP00000485244.1:p.Leu97Phe
ENST00000635828.1:c.289C>T ENSP00000490170.1:p.Leu97Phe
ENST00000637881.1:c.289C>T ENSP00000489879.1:p.Leu97Phe
ENST00000674046.1:c.289C>T ENSP00000501174.1:p.Leu97Phe
ENST00000379989.6:c.289C>T ENSP00000369325.3:p.Leu97Phe
ENST00000379996.7:c.289C>T ENSP00000369332.3:p.Leu97Phe
ENST00000463994.4:c.289C>T ENSP00000485184.1:p.Leu97Phe
ENST00000623535.1:c.289C>T ENSP00000485244.1:p.Leu97Phe
NM_001037343.1:c.289C>T NP_001032420.1:p.Leu97Phe
NM_003159.2:c.289C>T NP_003150.1:p.Leu97Phe
XM_011545569.1:c.289C>T XP_011543871.1:p.Leu97Phe
XM_011545570.1:c.157C>T XP_011543872.1:p.Leu53Phe
XR_950484.1:n.541C>T
NM_001323289.1:c.289C>T NP_001310218.1:p.Leu97Phe
NM_001323289.2:c.289C>T MANE Select NP_001310218.1:p.Leu97Phe
NM_001037343.2:c.289C>T NP_001032420.1:p.Leu97Phe
NM_003159.3:c.289C>T NP_003150.1:p.Leu97Phe