Canonical Allele Identifier: CA2417974479
Gene: CDKL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18604655G= , CM000685.2:g.18604655G= GRCh38
NC_000023.10:g.18622775G= , CM000685.1:g.18622775G= GRCh37
NC_000023.9:g.18532696G= NCBI36
NG_008475.1:g.184051G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000623535.2:c.1731G= MANE Select ENSP00000485244.1:p.Met577=
ENST00000635828.1:c.1731G= ENSP00000490170.1:p.Met577=
ENST00000674046.1:c.1731G= ENSP00000501174.1:p.Met577=
ENST00000379989.6:c.1731G= ENSP00000369325.3:p.Met577=
ENST00000379996.7:c.1731G= ENSP00000369332.3:p.Met577=
ENST00000463994.4:c.1731G= ENSP00000485184.1:p.Met577=
ENST00000623535.1:c.1731G= ENSP00000485244.1:p.Met577=
NM_001037343.1:c.1731G= NP_001032420.1:p.Met577=
NM_003159.2:c.1731G= NP_003150.1:p.Met577=
XM_011545569.1:c.1680G= XP_011543871.1:p.Met560=
XM_011545570.1:c.1599G= XP_011543872.1:p.Met533=
XR_950484.1:n.1983G=
NM_001323289.1:c.1731G= NP_001310218.1:p.Met577=
NM_001323289.2:c.1731G= MANE Select NP_001310218.1:p.Met577=
NM_001037343.2:c.1731G= NP_001032420.1:p.Met577=
NM_003159.3:c.1731G= NP_003150.1:p.Met577=