Canonical Allele Identifier: CA2819902188

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18644656_18644657insAG , CM000685.2:g.18644656_18644657insAG GRCh38
NC_000023.10:g.18662776_18662777insAG , CM000685.1:g.18662776_18662777insAG GRCh37
NC_000023.9:g.18572697_18572698insAG NCBI36
NG_008475.1:g.224052_224053insAG
NG_008659.3:g.37792_37793insCT , LRG_702:g.37792_37793insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000379984.4:c.327-32_327-31insCT (RS1) MANE Select ENSP00000369320.3:n.327-32_327-31insCT
ENST00000379984.3:c.327-32_327-31insCT (RS1) ENSP00000369320.3:n.327-32_327-31insCT
ENST00000379989.6:c.2714-1351_2714-1350insAG (CDKL5) ENSP00000369325.3:n.2714-1351_2714-1350insAG
ENST00000379996.7:c.2714-1351_2714-1350insAG (CDKL5) ENSP00000369332.3:n.2714-1351_2714-1350insAG
ENST00000476595.1:n.818-32_818-31insCT (RS1)
NM_000330.3:c.327-32_327-31insCT , LRG_702t1:c.327-32_327-31insCT (RS1) NP_000321.1:n.327-32_327-31insCT
NM_001037343.1:c.2714-1351_2714-1350insAG (CDKL5) NP_001032420.1:n.2714-1351_2714-1350insAG
NM_003159.2:c.2714-1351_2714-1350insAG (CDKL5) NP_003150.1:n.2714-1351_2714-1350insAG
XM_011545569.1:c.2786-1351_2786-1350insAG (CDKL5) XP_011543871.1:n.2786-1351_2786-1350insAG
XM_011545570.1:c.2705-1351_2705-1350insAG (CDKL5) XP_011543872.1:n.2705-1351_2705-1350insAG
XR_950484.1:n.3089-1351_3089-1350insAG (CDKL5)
NM_000330.4:c.327-32_327-31insCT (RS1) MANE Select NP_000321.1:n.327-32_327-31insCT
NM_001037343.2:c.2714-1351_2714-1350insAG (CDKL5) NP_001032420.1:n.2714-1351_2714-1350insAG
NM_003159.3:c.2714-1351_2714-1350insAG (CDKL5) NP_003150.1:n.2714-1351_2714-1350insAG