Canonical Allele Identifier: CA515471763

Gene: CDKL5

Linked Data

• MyVariant Identifiers: chrX:g.18622034C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18603914C>T , CM000685.2:g.18603914C>T	GRCh38
NC_000023.10:g.18622034C>T , CM000685.1:g.18622034C>T	GRCh37
NC_000023.9:g.18531955C>T	NCBI36
NG_008475.1:g.183310C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.990C>T MANE Select	ENSP00000485244.1:p.Gly330=
ENST00000635828.1:c.990C>T	ENSP00000490170.1:p.Gly330=
ENST00000637881.1:c.990C>T	ENSP00000489879.1:p.Gly330=
ENST00000674046.1:c.990C>T	ENSP00000501174.1:p.Gly330=
ENST00000379989.6:c.990C>T	ENSP00000369325.3:p.Gly330=
ENST00000379996.7:c.990C>T	ENSP00000369332.3:p.Gly330=
ENST00000463994.4:c.990C>T	ENSP00000485184.1:p.Gly330=
ENST00000623535.1:c.990C>T	ENSP00000485244.1:p.Gly330=
NM_001037343.1:c.990C>T	NP_001032420.1:p.Gly330=
NM_003159.2:c.990C>T	NP_003150.1:p.Gly330=
XM_011545569.1:c.939C>T	XP_011543871.1:p.Gly313=
XM_011545570.1:c.858C>T	XP_011543872.1:p.Gly286=
XR_950484.1:n.1242C>T
NM_001323289.1:c.990C>T	NP_001310218.1:p.Gly330=
NM_001323289.2:c.990C>T MANE Select	NP_001310218.1:p.Gly330=
NM_001037343.2:c.990C>T	NP_001032420.1:p.Gly330=
NM_003159.3:c.990C>T	NP_003150.1:p.Gly330=