Canonical Allele Identifier: CA2417987198

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18644292A= , CM000685.2:g.18644292A= GRCh38
NC_000023.10:g.18662412A= , CM000685.1:g.18662412A= GRCh37
NC_000023.9:g.18572333A= NCBI36
NG_008475.1:g.223688A=
NG_008659.3:g.38157T= , LRG_702:g.38157T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379984.4:c.522+138T= (RS1) MANE Select ENSP00000369320.3:n.522+138T=
ENST00000379984.3:c.522+138T= (RS1) ENSP00000369320.3:n.522+138T=
ENST00000379989.6:c.2714-1715A= (CDKL5) ENSP00000369325.3:n.2714-1715A=
ENST00000379996.7:c.2714-1715A= (CDKL5) ENSP00000369332.3:n.2714-1715A=
ENST00000476595.1:n.1013+138T= (RS1)
NM_000330.3:c.522+138T= , LRG_702t1:c.522+138T= (RS1) NP_000321.1:n.522+138T=
NM_001037343.1:c.2714-1715A= (CDKL5) NP_001032420.1:n.2714-1715A=
NM_003159.2:c.2714-1715A= (CDKL5) NP_003150.1:n.2714-1715A=
XM_011545569.1:c.2786-1715A= (CDKL5) XP_011543871.1:n.2786-1715A=
XM_011545570.1:c.2705-1715A= (CDKL5) XP_011543872.1:n.2705-1715A=
XR_950484.1:n.3089-1715A= (CDKL5)
NM_000330.4:c.522+138T= (RS1) MANE Select NP_000321.1:n.522+138T=
NM_001037343.2:c.2714-1715A= (CDKL5) NP_001032420.1:n.2714-1715A=
NM_003159.3:c.2714-1715A= (CDKL5) NP_003150.1:n.2714-1715A=