Canonical Allele Identifier: CA412367132
Gene: CDKL5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18628417C>A , CM000685.2:g.18628417C>A GRCh38
NC_000023.10:g.18646537C>A , CM000685.1:g.18646537C>A GRCh37
NC_000023.9:g.18556458C>A NCBI36
NG_008475.1:g.207813C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000623535.2:c.2543C>A MANE Select ENSP00000485244.1:p.Ala848Asp
ENST00000674046.1:c.2666C>A ENSP00000501174.1:p.Ala889Asp
ENST00000379989.6:c.2543C>A ENSP00000369325.3:p.Ala848Asp
ENST00000379996.7:c.2543C>A ENSP00000369332.3:p.Ala848Asp
ENST00000623535.1:c.2543C>A ENSP00000485244.1:p.Ala848Asp
NM_001037343.1:c.2543C>A NP_001032420.1:p.Ala848Asp
NM_003159.2:c.2543C>A NP_003150.1:p.Ala848Asp
XM_011545569.1:c.2615C>A XP_011543871.1:p.Ala872Asp
XM_011545570.1:c.2534C>A XP_011543872.1:p.Ala845Asp
XR_950484.1:n.2918C>A
NM_001323289.1:c.2543C>A NP_001310218.1:p.Ala848Asp
NM_001323289.2:c.2543C>A MANE Select NP_001310218.1:p.Ala848Asp
NM_001037343.2:c.2543C>A NP_001032420.1:p.Ala848Asp
NM_003159.3:c.2543C>A NP_003150.1:p.Ala848Asp