Canonical Allele Identifier: CA2417986343

Linked Data

dbSNP Id: rs1927585547
gnomAD v4: X-18641838-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18641838A>T , CM000685.2:g.18641838A>T GRCh38
NC_000023.10:g.18659958A>T , CM000685.1:g.18659958A>T GRCh37
NC_000023.9:g.18569879A>T NCBI36
NG_008475.1:g.221234A>T
NG_008659.3:g.40611T>A , LRG_702:g.40611T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379984.4:c.*166T>A (RS1) MANE Select ENSP00000369320.3:n.*166T>A
ENST00000379984.3:c.*166T>A (RS1) ENSP00000369320.3:n.*166T>A
ENST00000379989.6:c.2714-4169A>T (CDKL5) ENSP00000369325.3:n.2714-4169A>T
ENST00000379996.7:c.2714-4169A>T (CDKL5) ENSP00000369332.3:n.2714-4169A>T
NM_000330.3:c.*166T>A , LRG_702t1:c.*166T>A (RS1) NP_000321.1:n.*166T>A
NM_001037343.1:c.2714-4169A>T (CDKL5) NP_001032420.1:n.2714-4169A>T
NM_003159.2:c.2714-4169A>T (CDKL5) NP_003150.1:n.2714-4169A>T
XM_011545569.1:c.2786-4169A>T (CDKL5) XP_011543871.1:n.2786-4169A>T
XM_011545570.1:c.2705-4169A>T (CDKL5) XP_011543872.1:n.2705-4169A>T
XR_950484.1:n.3089-4169A>T (CDKL5)
NM_000330.4:c.*166T>A (RS1) MANE Select NP_000321.1:n.*166T>A
NM_001037343.2:c.2714-4169A>T (CDKL5) NP_001032420.1:n.2714-4169A>T
NM_003159.3:c.2714-4169A>T (CDKL5) NP_003150.1:n.2714-4169A>T