Canonical Allele Identifier: CA412367076

Gene: CDKL5

Linked Data

• MyVariant Identifiers: chrX:g.18646526T>G (hg19) ; chrX:g.18628406T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18628406T>G , CM000685.2:g.18628406T>G	GRCh38
NC_000023.10:g.18646526T>G , CM000685.1:g.18646526T>G	GRCh37
NC_000023.9:g.18556447T>G	NCBI36
NG_008475.1:g.207802T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.2532T>G MANE Select	ENSP00000485244.1:p.His844Gln
ENST00000674046.1:c.2655T>G	ENSP00000501174.1:p.His885Gln
ENST00000379989.6:c.2532T>G	ENSP00000369325.3:p.His844Gln
ENST00000379996.7:c.2532T>G	ENSP00000369332.3:p.His844Gln
ENST00000623535.1:c.2532T>G	ENSP00000485244.1:p.His844Gln
NM_001037343.1:c.2532T>G	NP_001032420.1:p.His844Gln
NM_003159.2:c.2532T>G	NP_003150.1:p.His844Gln
XM_011545569.1:c.2604T>G	XP_011543871.1:p.His868Gln
XM_011545570.1:c.2523T>G	XP_011543872.1:p.His841Gln
XR_950484.1:n.2907T>G
NM_001323289.1:c.2532T>G	NP_001310218.1:p.His844Gln
NM_001323289.2:c.2532T>G MANE Select	NP_001310218.1:p.His844Gln
NM_001037343.2:c.2532T>G	NP_001032420.1:p.His844Gln
NM_003159.3:c.2532T>G	NP_003150.1:p.His844Gln