Canonical Allele Identifier: CA412368978

Gene: CDKL5

Linked Data

• ClinVar Variation Id: 2136156
• ClinVar RCV Id: RCV003037030
• MyVariant Identifiers: chrX:g.18646781G>T (hg19) ; chrX:g.18628661G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18628661G>T , CM000685.2:g.18628661G>T	GRCh38
NC_000023.10:g.18646781G>T , CM000685.1:g.18646781G>T	GRCh37
NC_000023.9:g.18556702G>T	NCBI36
NG_008475.1:g.208057G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.2787G>T MANE Select	ENSP00000485244.1:p.Gln929His
ENST00000674046.1:c.2910G>T	ENSP00000501174.1:p.Gln970His
ENST00000379989.6:c.2713+74G>T	ENSP00000369325.3:n.2713+74G>T
ENST00000379996.7:c.2713+74G>T	ENSP00000369332.3:n.2713+74G>T
ENST00000623535.1:c.2787G>T	ENSP00000485244.1:p.Gln929His
NM_001037343.1:c.2713+74G>T	NP_001032420.1:n.2713+74G>T
NM_003159.2:c.2713+74G>T	NP_003150.1:n.2713+74G>T
XM_011545569.1:c.2785+74G>T	XP_011543871.1:n.2785+74G>T
XM_011545570.1:c.2704+74G>T	XP_011543872.1:n.2704+74G>T
XR_950484.1:n.3088+74G>T
NM_001323289.1:c.2787G>T	NP_001310218.1:p.Gln929His
NM_001323289.2:c.2787G>T MANE Select	NP_001310218.1:p.Gln929His
NM_001037343.2:c.2713+74G>T	NP_001032420.1:n.2713+74G>T
NM_003159.3:c.2713+74G>T	NP_003150.1:n.2713+74G>T