Canonical Allele Identifier: CA412367039

Gene: CDKL5

Linked Data

• MyVariant Identifiers: chrX:g.18646520G>T (hg19) ; chrX:g.18628400G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18628400G>T , CM000685.2:g.18628400G>T	GRCh38
NC_000023.10:g.18646520G>T , CM000685.1:g.18646520G>T	GRCh37
NC_000023.9:g.18556441G>T	NCBI36
NG_008475.1:g.207796G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.2526G>T MANE Select	ENSP00000485244.1:p.Leu842Phe
ENST00000674046.1:c.2649G>T	ENSP00000501174.1:p.Leu883Phe
ENST00000379989.6:c.2526G>T	ENSP00000369325.3:p.Leu842Phe
ENST00000379996.7:c.2526G>T	ENSP00000369332.3:p.Leu842Phe
ENST00000623535.1:c.2526G>T	ENSP00000485244.1:p.Leu842Phe
NM_001037343.1:c.2526G>T	NP_001032420.1:p.Leu842Phe
NM_003159.2:c.2526G>T	NP_003150.1:p.Leu842Phe
XM_011545569.1:c.2598G>T	XP_011543871.1:p.Leu866Phe
XM_011545570.1:c.2517G>T	XP_011543872.1:p.Leu839Phe
XR_950484.1:n.2901G>T
NM_001323289.1:c.2526G>T	NP_001310218.1:p.Leu842Phe
NM_001323289.2:c.2526G>T MANE Select	NP_001310218.1:p.Leu842Phe
NM_001037343.2:c.2526G>T	NP_001032420.1:p.Leu842Phe
NM_003159.3:c.2526G>T	NP_003150.1:p.Leu842Phe