Canonical Allele Identifier: CA2537535743

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18644397_18644398del , CM000685.2:g.18644397_18644398del GRCh38
NC_000023.10:g.18662517_18662518del , CM000685.1:g.18662517_18662518del GRCh37
NC_000023.9:g.18572438_18572439del NCBI36
NG_008475.1:g.223793_223794del
NG_008659.3:g.38052_38053del , LRG_702:g.38052_38053del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379984.4:c.522+33_522+34del (RS1) MANE Select ENSP00000369320.3:n.522+33_522+34del
ENST00000379984.3:c.522+33_522+34del (RS1) ENSP00000369320.3:n.522+33_522+34del
ENST00000379989.6:c.2714-1610_2714-1609del (CDKL5) ENSP00000369325.3:n.2714-1610_2714-1609del
ENST00000379996.7:c.2714-1610_2714-1609del (CDKL5) ENSP00000369332.3:n.2714-1610_2714-1609del
ENST00000476595.1:n.1013+33_1013+34del (RS1)
NM_000330.3:c.522+33_522+34del , LRG_702t1:c.522+33_522+34del (RS1) NP_000321.1:n.522+33_522+34del
NM_001037343.1:c.2714-1610_2714-1609del (CDKL5) NP_001032420.1:n.2714-1610_2714-1609del
NM_003159.2:c.2714-1610_2714-1609del (CDKL5) NP_003150.1:n.2714-1610_2714-1609del
XM_011545569.1:c.2786-1610_2786-1609del (CDKL5) XP_011543871.1:n.2786-1610_2786-1609del
XM_011545570.1:c.2705-1610_2705-1609del (CDKL5) XP_011543872.1:n.2705-1610_2705-1609del
XR_950484.1:n.3089-1610_3089-1609del (CDKL5)
NM_000330.4:c.522+33_522+34del (RS1) MANE Select NP_000321.1:n.522+33_522+34del
NM_001037343.2:c.2714-1610_2714-1609del (CDKL5) NP_001032420.1:n.2714-1610_2714-1609del
NM_003159.3:c.2714-1610_2714-1609del (CDKL5) NP_003150.1:n.2714-1610_2714-1609del