Canonical Allele Identifier: CA515470731
Gene: CDKL5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.18646629C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18628509C>T , CM000685.2:g.18628509C>T GRCh38
NC_000023.10:g.18646629C>T , CM000685.1:g.18646629C>T GRCh37
NC_000023.9:g.18556550C>T NCBI36
NG_008475.1:g.207905C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000623535.2:c.2635C>T MANE Select ENSP00000485244.1:p.Leu879=
ENST00000674046.1:c.2758C>T ENSP00000501174.1:p.Leu920=
ENST00000379989.6:c.2635C>T ENSP00000369325.3:p.Leu879=
ENST00000379996.7:c.2635C>T ENSP00000369332.3:p.Leu879=
ENST00000623535.1:c.2635C>T ENSP00000485244.1:p.Leu879=
NM_001037343.1:c.2635C>T NP_001032420.1:p.Leu879=
NM_003159.2:c.2635C>T NP_003150.1:p.Leu879=
XM_011545569.1:c.2707C>T XP_011543871.1:p.Leu903=
XM_011545570.1:c.2626C>T XP_011543872.1:p.Leu876=
XR_950484.1:n.3010C>T
NM_001323289.1:c.2635C>T NP_001310218.1:p.Leu879=
NM_001323289.2:c.2635C>T MANE Select NP_001310218.1:p.Leu879=
NM_001037343.2:c.2635C>T NP_001032420.1:p.Leu879=
NM_003159.3:c.2635C>T NP_003150.1:p.Leu879=