Canonical Allele Identifier: CA218968

Linked Data

ClinVar Variation Id: 68075
ClinVar RCV Id: RCV000058879
dbSNP Id: rs199469699

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18644520_18644567dup , CM000685.2:g.18644520_18644567dup GRCh38
NC_000023.10:g.18662640_18662687dup , CM000685.1:g.18662640_18662687dup GRCh37
NC_000023.9:g.18572561_18572608dup NCBI36
NG_008475.1:g.223916_223963dup
NG_008659.3:g.37884_37931dup , LRG_702:g.37884_37931dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000379984.4:c.387_434dup (RS1) MANE Select ENSP00000369320.3:p.Ile144_Asp145insGluIleLysValIleSerGlyIleL...
ENST00000379984.3:c.387_434dup (RS1) ENSP00000369320.3:p.Ile144_Asp145insGluIleLysValIleSerGlyIleL...
ENST00000379989.6:c.2714-1487_2714-1440dup (CDKL5) ENSP00000369325.3:n.2714-1487_2714-1440dup
ENST00000379996.7:c.2714-1487_2714-1440dup (CDKL5) ENSP00000369332.3:n.2714-1487_2714-1440dup
ENST00000476595.1:n.878_925dup (RS1)
NM_000330.3:c.387_434dup , LRG_702t1:c.387_434dup (RS1) NP_000321.1:p.Ile144_Asp145insGluIleLysValIleSerGlyIleLeuThrG...
NM_001037343.1:c.2714-1487_2714-1440dup (CDKL5) NP_001032420.1:n.2714-1487_2714-1440dup
NM_003159.2:c.2714-1487_2714-1440dup (CDKL5) NP_003150.1:n.2714-1487_2714-1440dup
XM_011545569.1:c.2786-1487_2786-1440dup (CDKL5) XP_011543871.1:n.2786-1487_2786-1440dup
XM_011545570.1:c.2705-1487_2705-1440dup (CDKL5) XP_011543872.1:n.2705-1487_2705-1440dup
XR_950484.1:n.3089-1487_3089-1440dup (CDKL5)
NM_000330.4:c.387_434dup (RS1) MANE Select NP_000321.1:p.Ile144_Asp145insGluIleLysValIleSerGlyIleLeuThrG...
NM_001037343.2:c.2714-1487_2714-1440dup (CDKL5) NP_001032420.1:n.2714-1487_2714-1440dup
NM_003159.3:c.2714-1487_2714-1440dup (CDKL5) NP_003150.1:n.2714-1487_2714-1440dup