Canonical Allele Identifier: CA327011141

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18641870del , CM000685.2:g.18641870del GRCh38
NC_000023.10:g.18659990del , CM000685.1:g.18659990del GRCh37
NC_000023.9:g.18569911del NCBI36
NG_008475.1:g.221266del
NG_008659.3:g.40591del , LRG_702:g.40591del

Transcript Alleles

HGVS Amino-acid Change
NM_000330.4:c.*146del (RS1) MANE Select NP_000321.1:n.*146del
ENST00000379984.4:c.*146del (RS1) MANE Select ENSP00000369320.3:n.*146del
NM_000330.3:c.*146del , LRG_702t1:c.*146del (RS1) NP_000321.1:n.*146del
NM_001037343.1:c.2714-4137del (CDKL5) NP_001032420.1:n.2714-4137del
NM_001037343.2:c.2714-4137del (CDKL5) NP_001032420.1:n.2714-4137del
NM_003159.2:c.2714-4137del (CDKL5) NP_003150.1:n.2714-4137del
NM_003159.3:c.2714-4137del (CDKL5) NP_003150.1:n.2714-4137del
ENST00000379984.3:c.*146del (RS1) ENSP00000369320.3:n.*146del
ENST00000379989.6:c.2714-4137del (CDKL5) ENSP00000369325.3:n.2714-4137del
ENST00000379996.7:c.2714-4137del (CDKL5) ENSP00000369332.3:n.2714-4137del
XM_011545569.1:c.2786-4137del (CDKL5) XP_011543871.1:n.2786-4137del
XM_011545570.1:c.2705-4137del (CDKL5) XP_011543872.1:n.2705-4137del
XR_950484.1:n.3089-4137del (CDKL5)