Canonical Allele Identifier: CA2417987292

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18644535_18644536delinsCT , CM000685.2:g.18644535_18644536delinsCT GRCh38
NC_000023.10:g.18662655_18662656delinsCT , CM000685.1:g.18662655_18662656delinsCT GRCh37
NC_000023.9:g.18572576_18572577delinsCT NCBI36
NG_008475.1:g.223931_223932delinsCT
NG_008659.3:g.37913_37914delinsAG , LRG_702:g.37913_37914delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000379984.4:c.416_417delinsAG (RS1) MANE Select ENSP00000369320.3:p.Gln139=
ENST00000379984.3:c.416_417delinsAG (RS1) ENSP00000369320.3:p.Gln139=
ENST00000379989.6:c.2714-1472_2714-1471delinsCT (CDKL5) ENSP00000369325.3:n.2714-1472_2714-1471delinsCT
ENST00000379996.7:c.2714-1472_2714-1471delinsCT (CDKL5) ENSP00000369332.3:n.2714-1472_2714-1471delinsCT
ENST00000476595.1:n.907_908delinsAG (RS1)
NM_000330.3:c.416_417delinsAG , LRG_702t1:c.416_417delinsAG (RS1) NP_000321.1:p.Gln139=
NM_001037343.1:c.2714-1472_2714-1471delinsCT (CDKL5) NP_001032420.1:n.2714-1472_2714-1471delinsCT
NM_003159.2:c.2714-1472_2714-1471delinsCT (CDKL5) NP_003150.1:n.2714-1472_2714-1471delinsCT
XM_011545569.1:c.2786-1472_2786-1471delinsCT (CDKL5) XP_011543871.1:n.2786-1472_2786-1471delinsCT
XM_011545570.1:c.2705-1472_2705-1471delinsCT (CDKL5) XP_011543872.1:n.2705-1472_2705-1471delinsCT
XR_950484.1:n.3089-1472_3089-1471delinsCT (CDKL5)
NM_000330.4:c.416_417delinsAG (RS1) MANE Select NP_000321.1:p.Gln139=
NM_001037343.2:c.2714-1472_2714-1471delinsCT (CDKL5) NP_001032420.1:n.2714-1472_2714-1471delinsCT
NM_003159.3:c.2714-1472_2714-1471delinsCT (CDKL5) NP_003150.1:n.2714-1472_2714-1471delinsCT