Canonical Allele Identifier: CA2819901345

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18641936_18641938del , CM000685.2:g.18641936_18641938del GRCh38
NC_000023.10:g.18660056_18660058del , CM000685.1:g.18660056_18660058del GRCh37
NC_000023.9:g.18569977_18569979del NCBI36
NG_008475.1:g.221332_221334del
NG_008659.3:g.40511_40513del , LRG_702:g.40511_40513del

Transcript Alleles

HGVS Amino-acid change
ENST00000379984.4:c.*66_*68del (RS1) MANE Select ENSP00000369320.3:n.*66_*68del
ENST00000379984.3:c.*66_*68del (RS1) ENSP00000369320.3:n.*66_*68del
ENST00000379989.6:c.2714-4071_2714-4069del (CDKL5) ENSP00000369325.3:n.2714-4071_2714-4069del
ENST00000379996.7:c.2714-4071_2714-4069del (CDKL5) ENSP00000369332.3:n.2714-4071_2714-4069del
ENST00000476595.1:n.1232_1234del (RS1)
NM_000330.3:c.*66_*68del , LRG_702t1:c.*66_*68del (RS1) NP_000321.1:n.*66_*68del
NM_001037343.1:c.2714-4071_2714-4069del (CDKL5) NP_001032420.1:n.2714-4071_2714-4069del
NM_003159.2:c.2714-4071_2714-4069del (CDKL5) NP_003150.1:n.2714-4071_2714-4069del
XM_011545569.1:c.2786-4071_2786-4069del (CDKL5) XP_011543871.1:n.2786-4071_2786-4069del
XM_011545570.1:c.2705-4071_2705-4069del (CDKL5) XP_011543872.1:n.2705-4071_2705-4069del
XR_950484.1:n.3089-4071_3089-4069del (CDKL5)
NM_000330.4:c.*66_*68del (RS1) MANE Select NP_000321.1:n.*66_*68del
NM_001037343.2:c.2714-4071_2714-4069del (CDKL5) NP_001032420.1:n.2714-4071_2714-4069del
NM_003159.3:c.2714-4071_2714-4069del (CDKL5) NP_003150.1:n.2714-4071_2714-4069del