Canonical Allele Identifier: CA515471859
Gene: CDKL5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.18622055T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18603935T>A , CM000685.2:g.18603935T>A GRCh38
NC_000023.10:g.18622055T>A , CM000685.1:g.18622055T>A GRCh37
NC_000023.9:g.18531976T>A NCBI36
NG_008475.1:g.183331T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000623535.2:c.1011T>A MANE Select ENSP00000485244.1:p.Ser337=
ENST00000635828.1:c.1011T>A ENSP00000490170.1:p.Ser337=
ENST00000637881.1:c.1011T>A ENSP00000489879.1:p.Ser337=
ENST00000674046.1:c.1011T>A ENSP00000501174.1:p.Ser337=
ENST00000379989.6:c.1011T>A ENSP00000369325.3:p.Ser337=
ENST00000379996.7:c.1011T>A ENSP00000369332.3:p.Ser337=
ENST00000463994.4:c.1011T>A ENSP00000485184.1:p.Ser337=
ENST00000623535.1:c.1011T>A ENSP00000485244.1:p.Ser337=
NM_001037343.1:c.1011T>A NP_001032420.1:p.Ser337=
NM_003159.2:c.1011T>A NP_003150.1:p.Ser337=
XM_011545569.1:c.960T>A XP_011543871.1:p.Ser320=
XM_011545570.1:c.879T>A XP_011543872.1:p.Ser293=
XR_950484.1:n.1263T>A
NM_001323289.1:c.1011T>A NP_001310218.1:p.Ser337=
NM_001323289.2:c.1011T>A MANE Select NP_001310218.1:p.Ser337=
NM_001037343.2:c.1011T>A NP_001032420.1:p.Ser337=
NM_003159.3:c.1011T>A NP_003150.1:p.Ser337=