Canonical Allele Identifier: CA412352089
Gene: CDKL5 HGNC NCBI

Linked Data

ClinVar Variation Id: 834731
ClinVar RCV Id: RCV001035473
dbSNP Id: rs786204986

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18584262G>C , CM000685.2:g.18584262G>C GRCh38
NC_000023.10:g.18602382G>C , CM000685.1:g.18602382G>C GRCh37
NC_000023.9:g.18512303G>C NCBI36
NG_008475.1:g.163658G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000623535.2:c.464-1G>C MANE Select ENSP00000485244.1:n.464-1G>C
ENST00000635828.1:c.464-1G>C ENSP00000490170.1:n.464-1G>C
ENST00000637881.1:c.464-1G>C ENSP00000489879.1:n.464-1G>C
ENST00000674046.1:c.464-1G>C ENSP00000501174.1:n.464-1G>C
ENST00000379989.6:c.464-1G>C ENSP00000369325.3:n.464-1G>C
ENST00000379996.7:c.464-1G>C ENSP00000369332.3:n.464-1G>C
ENST00000463994.4:c.464-1G>C ENSP00000485184.1:n.464-1G>C
ENST00000623535.1:c.464-1G>C ENSP00000485244.1:n.464-1G>C
NM_001037343.1:c.464-1G>C NP_001032420.1:n.464-1G>C
NM_003159.2:c.464-1G>C NP_003150.1:n.464-1G>C
XM_011545569.1:c.464-1G>C XP_011543871.1:n.464-1G>C
XM_011545570.1:c.332-1G>C XP_011543872.1:n.332-1G>C
XR_950484.1:n.716-1G>C
NM_001323289.1:c.464-1G>C NP_001310218.1:n.464-1G>C
NM_001323289.2:c.464-1G>C MANE Select NP_001310218.1:n.464-1G>C
NM_001037343.2:c.464-1G>C NP_001032420.1:n.464-1G>C
NM_003159.3:c.464-1G>C NP_003150.1:n.464-1G>C