Canonical Allele Identifier: CA515470563
Gene: CDKL5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.18646518T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18628398T>C , CM000685.2:g.18628398T>C GRCh38
NC_000023.10:g.18646518T>C , CM000685.1:g.18646518T>C GRCh37
NC_000023.9:g.18556439T>C NCBI36
NG_008475.1:g.207794T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000623535.2:c.2524T>C MANE Select ENSP00000485244.1:p.Leu842=
ENST00000674046.1:c.2647T>C ENSP00000501174.1:p.Leu883=
ENST00000379989.6:c.2524T>C ENSP00000369325.3:p.Leu842=
ENST00000379996.7:c.2524T>C ENSP00000369332.3:p.Leu842=
ENST00000623535.1:c.2524T>C ENSP00000485244.1:p.Leu842=
NM_001037343.1:c.2524T>C NP_001032420.1:p.Leu842=
NM_003159.2:c.2524T>C NP_003150.1:p.Leu842=
XM_011545569.1:c.2596T>C XP_011543871.1:p.Leu866=
XM_011545570.1:c.2515T>C XP_011543872.1:p.Leu839=
XR_950484.1:n.2899T>C
NM_001323289.1:c.2524T>C NP_001310218.1:p.Leu842=
NM_001323289.2:c.2524T>C MANE Select NP_001310218.1:p.Leu842=
NM_001037343.2:c.2524T>C NP_001032420.1:p.Leu842=
NM_003159.3:c.2524T>C NP_003150.1:p.Leu842=