Canonical Allele Identifier: CA226673

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18647205G>C , CM000685.2:g.18647205G>C GRCh38
NC_000023.10:g.18665325G>C , CM000685.1:g.18665325G>C GRCh37
NC_000023.9:g.18575246G>C NCBI36
NG_008475.1:g.226601G>C
NG_008659.3:g.35244C>G , LRG_702:g.35244C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000330.4:c.312C>G (RS1) MANE Select NP_000321.1:p.Asn104Lys
ENST00000379984.4:c.312C>G (RS1) MANE Select ENSP00000369320.3:p.Asn104Lys
NM_000330.3:c.312C>G , LRG_702t1:c.312C>G (RS1) NP_000321.1:p.Asn104Lys
NM_001037343.1:c.2797+1115G>C (CDKL5) NP_001032420.1:n.2797+1115G>C
NM_001037343.2:c.2797+1115G>C (CDKL5) NP_001032420.1:n.2797+1115G>C
NM_003159.2:c.2797+1115G>C (CDKL5) NP_003150.1:n.2797+1115G>C
NM_003159.3:c.2797+1115G>C (CDKL5) NP_003150.1:n.2797+1115G>C
ENST00000379984.3:c.312C>G (RS1) ENSP00000369320.3:p.Asn104Lys
ENST00000379989.6:c.2797+1115G>C (CDKL5) ENSP00000369325.3:n.2797+1115G>C
ENST00000379996.7:c.2797+1115G>C (CDKL5) ENSP00000369332.3:n.2797+1115G>C
ENST00000476595.1:n.803C>G (RS1)
XM_011545569.1:c.2869+1115G>C (CDKL5) XP_011543871.1:n.2869+1115G>C
XM_011545570.1:c.2788+1115G>C (CDKL5) XP_011543872.1:n.2788+1115G>C
XR_950484.1:n.3172+1115G>C (CDKL5)