Canonical Allele Identifier: CA2819901256

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18641833_18641837del , CM000685.2:g.18641833_18641837del GRCh38
NC_000023.10:g.18659953_18659957del , CM000685.1:g.18659953_18659957del GRCh37
NC_000023.9:g.18569874_18569878del NCBI36
NG_008475.1:g.221229_221233del
NG_008659.3:g.40612_40616del , LRG_702:g.40612_40616del

Transcript Alleles

HGVS Amino-acid change
ENST00000379984.4:c.*167_*171del (RS1) MANE Select ENSP00000369320.3:n.*167_*171del
ENST00000379984.3:c.*167_*171del (RS1) ENSP00000369320.3:n.*167_*171del
ENST00000379989.6:c.2714-4174_2714-4170del (CDKL5) ENSP00000369325.3:n.2714-4174_2714-4170del
ENST00000379996.7:c.2714-4174_2714-4170del (CDKL5) ENSP00000369332.3:n.2714-4174_2714-4170del
NM_000330.3:c.*167_*171del , LRG_702t1:c.*167_*171del (RS1) NP_000321.1:n.*167_*171del
NM_001037343.1:c.2714-4174_2714-4170del (CDKL5) NP_001032420.1:n.2714-4174_2714-4170del
NM_003159.2:c.2714-4174_2714-4170del (CDKL5) NP_003150.1:n.2714-4174_2714-4170del
XM_011545569.1:c.2786-4174_2786-4170del (CDKL5) XP_011543871.1:n.2786-4174_2786-4170del
XM_011545570.1:c.2705-4174_2705-4170del (CDKL5) XP_011543872.1:n.2705-4174_2705-4170del
XR_950484.1:n.3089-4174_3089-4170del (CDKL5)
NM_000330.4:c.*167_*171del (RS1) MANE Select NP_000321.1:n.*167_*171del
NM_001037343.2:c.2714-4174_2714-4170del (CDKL5) NP_001032420.1:n.2714-4174_2714-4170del
NM_003159.3:c.2714-4174_2714-4170del (CDKL5) NP_003150.1:n.2714-4174_2714-4170del