Canonical Allele Identifier: CA515470592
Gene: CDKL5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.18646556C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18628436C>A , CM000685.2:g.18628436C>A GRCh38
NC_000023.10:g.18646556C>A , CM000685.1:g.18646556C>A GRCh37
NC_000023.9:g.18556477C>A NCBI36
NG_008475.1:g.207832C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000623535.2:c.2562C>A MANE Select ENSP00000485244.1:p.Ser854=
ENST00000674046.1:c.2685C>A ENSP00000501174.1:p.Ser895=
ENST00000379989.6:c.2562C>A ENSP00000369325.3:p.Ser854=
ENST00000379996.7:c.2562C>A ENSP00000369332.3:p.Ser854=
ENST00000623535.1:c.2562C>A ENSP00000485244.1:p.Ser854=
NM_001037343.1:c.2562C>A NP_001032420.1:p.Ser854=
NM_003159.2:c.2562C>A NP_003150.1:p.Ser854=
XM_011545569.1:c.2634C>A XP_011543871.1:p.Ser878=
XM_011545570.1:c.2553C>A XP_011543872.1:p.Ser851=
XR_950484.1:n.2937C>A
NM_001323289.1:c.2562C>A NP_001310218.1:p.Ser854=
NM_001323289.2:c.2562C>A MANE Select NP_001310218.1:p.Ser854=
NM_001037343.2:c.2562C>A NP_001032420.1:p.Ser854=
NM_003159.3:c.2562C>A NP_003150.1:p.Ser854=