Canonical Allele Identifier: CA515470227

Gene: CDKL5

Linked Data

• MyVariant Identifiers: chrX:g.18637996T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18619876T>G , CM000685.2:g.18619876T>G	GRCh38
NC_000023.10:g.18637996T>G , CM000685.1:g.18637996T>G	GRCh37
NC_000023.9:g.18547917T>G	NCBI36
NG_008475.1:g.199272T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000623535.2:c.2286T>G MANE Select	ENSP00000485244.1:p.Pro762=
ENST00000635828.1:c.2286T>G	ENSP00000490170.1:p.Pro762=
ENST00000674046.1:c.2286T>G	ENSP00000501174.1:p.Pro762=
ENST00000379989.6:c.2286T>G	ENSP00000369325.3:p.Pro762=
ENST00000379996.7:c.2286T>G	ENSP00000369332.3:p.Pro762=
ENST00000463994.4:c.2286T>G	ENSP00000485184.1:p.Pro762=
ENST00000623535.1:c.2286T>G	ENSP00000485244.1:p.Pro762=
NM_001037343.1:c.2286T>G	NP_001032420.1:p.Pro762=
NM_003159.2:c.2286T>G	NP_003150.1:p.Pro762=
XM_011545569.1:c.2235T>G	XP_011543871.1:p.Pro745=
XM_011545570.1:c.2154T>G	XP_011543872.1:p.Pro718=
XR_950484.1:n.2538T>G
NM_001323289.1:c.2286T>G	NP_001310218.1:p.Pro762=
NM_001323289.2:c.2286T>G MANE Select	NP_001310218.1:p.Pro762=
NM_001037343.2:c.2286T>G	NP_001032420.1:p.Pro762=
NM_003159.3:c.2286T>G	NP_003150.1:p.Pro762=