Canonical Allele Identifier: CA2417987352

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18644662_18644663delinsCT , CM000685.2:g.18644662_18644663delinsCT GRCh38
NC_000023.10:g.18662782_18662783delinsCT , CM000685.1:g.18662782_18662783delinsCT GRCh37
NC_000023.9:g.18572703_18572704delinsCT NCBI36
NG_008475.1:g.224058_224059delinsCT
NG_008659.3:g.37786_37787delinsAG , LRG_702:g.37786_37787delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000379984.4:c.327-38_327-37delinsAG (RS1) MANE Select ENSP00000369320.3:n.327-38_327-37delinsAG
ENST00000379984.3:c.327-38_327-37delinsAG (RS1) ENSP00000369320.3:n.327-38_327-37delinsAG
ENST00000379989.6:c.2714-1345_2714-1344delinsCT (CDKL5) ENSP00000369325.3:n.2714-1345_2714-1344delinsCT
ENST00000379996.7:c.2714-1345_2714-1344delinsCT (CDKL5) ENSP00000369332.3:n.2714-1345_2714-1344delinsCT
ENST00000476595.1:n.818-38_818-37delinsAG (RS1)
NM_000330.3:c.327-38_327-37delinsAG , LRG_702t1:c.327-38_327-37delinsAG (RS1) NP_000321.1:n.327-38_327-37delinsAG
NM_001037343.1:c.2714-1345_2714-1344delinsCT (CDKL5) NP_001032420.1:n.2714-1345_2714-1344delinsCT
NM_003159.2:c.2714-1345_2714-1344delinsCT (CDKL5) NP_003150.1:n.2714-1345_2714-1344delinsCT
XM_011545569.1:c.2786-1345_2786-1344delinsCT (CDKL5) XP_011543871.1:n.2786-1345_2786-1344delinsCT
XM_011545570.1:c.2705-1345_2705-1344delinsCT (CDKL5) XP_011543872.1:n.2705-1345_2705-1344delinsCT
XR_950484.1:n.3089-1345_3089-1344delinsCT (CDKL5)
NM_000330.4:c.327-38_327-37delinsAG (RS1) MANE Select NP_000321.1:n.327-38_327-37delinsAG
NM_001037343.2:c.2714-1345_2714-1344delinsCT (CDKL5) NP_001032420.1:n.2714-1345_2714-1344delinsCT
NM_003159.3:c.2714-1345_2714-1344delinsCT (CDKL5) NP_003150.1:n.2714-1345_2714-1344delinsCT