Canonical Allele Identifier: CA2819902173

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18644640_18644641insACA , CM000685.2:g.18644640_18644641insACA GRCh38
NC_000023.10:g.18662760_18662761insACA , CM000685.1:g.18662760_18662761insACA GRCh37
NC_000023.9:g.18572681_18572682insACA NCBI36
NG_008475.1:g.224036_224037insACA
NG_008659.3:g.37808_37809insTGT , LRG_702:g.37808_37809insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000379984.4:c.327-16_327-15insTGT (RS1) MANE Select ENSP00000369320.3:n.327-16_327-15insTGT
ENST00000379984.3:c.327-16_327-15insTGT (RS1) ENSP00000369320.3:n.327-16_327-15insTGT
ENST00000379989.6:c.2714-1367_2714-1366insACA (CDKL5) ENSP00000369325.3:n.2714-1367_2714-1366insACA
ENST00000379996.7:c.2714-1367_2714-1366insACA (CDKL5) ENSP00000369332.3:n.2714-1367_2714-1366insACA
ENST00000476595.1:n.818-16_818-15insTGT (RS1)
NM_000330.3:c.327-16_327-15insTGT , LRG_702t1:c.327-16_327-15insTGT (RS1) NP_000321.1:n.327-16_327-15insTGT
NM_001037343.1:c.2714-1367_2714-1366insACA (CDKL5) NP_001032420.1:n.2714-1367_2714-1366insACA
NM_003159.2:c.2714-1367_2714-1366insACA (CDKL5) NP_003150.1:n.2714-1367_2714-1366insACA
XM_011545569.1:c.2786-1367_2786-1366insACA (CDKL5) XP_011543871.1:n.2786-1367_2786-1366insACA
XM_011545570.1:c.2705-1367_2705-1366insACA (CDKL5) XP_011543872.1:n.2705-1367_2705-1366insACA
XR_950484.1:n.3089-1367_3089-1366insACA (CDKL5)
NM_000330.4:c.327-16_327-15insTGT (RS1) MANE Select NP_000321.1:n.327-16_327-15insTGT
NM_001037343.2:c.2714-1367_2714-1366insACA (CDKL5) NP_001032420.1:n.2714-1367_2714-1366insACA
NM_003159.3:c.2714-1367_2714-1366insACA (CDKL5) NP_003150.1:n.2714-1367_2714-1366insACA