Canonical Allele Identifier: CA2693227777

Linked Data

gnomAD v4: X-18641916-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18641916C>A , CM000685.2:g.18641916C>A GRCh38
NC_000023.10:g.18660036C>A , CM000685.1:g.18660036C>A GRCh37
NC_000023.9:g.18569957C>A NCBI36
NG_008475.1:g.221312C>A
NG_008659.3:g.40533G>T , LRG_702:g.40533G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379984.4:c.*88G>T (RS1) MANE Select ENSP00000369320.3:n.*88G>T
ENST00000379984.3:c.*88G>T (RS1) ENSP00000369320.3:n.*88G>T
ENST00000379989.6:c.2714-4091C>A (CDKL5) ENSP00000369325.3:n.2714-4091C>A
ENST00000379996.7:c.2714-4091C>A (CDKL5) ENSP00000369332.3:n.2714-4091C>A
NM_000330.3:c.*88G>T , LRG_702t1:c.*88G>T (RS1) NP_000321.1:n.*88G>T
NM_001037343.1:c.2714-4091C>A (CDKL5) NP_001032420.1:n.2714-4091C>A
NM_003159.2:c.2714-4091C>A (CDKL5) NP_003150.1:n.2714-4091C>A
XM_011545569.1:c.2786-4091C>A (CDKL5) XP_011543871.1:n.2786-4091C>A
XM_011545570.1:c.2705-4091C>A (CDKL5) XP_011543872.1:n.2705-4091C>A
XR_950484.1:n.3089-4091C>A (CDKL5)
NM_000330.4:c.*88G>T (RS1) MANE Select NP_000321.1:n.*88G>T
NM_001037343.2:c.2714-4091C>A (CDKL5) NP_001032420.1:n.2714-4091C>A
NM_003159.3:c.2714-4091C>A (CDKL5) NP_003150.1:n.2714-4091C>A