Canonical Allele Identifier: CA515628012

Gene: CDKL5

Linked Data

• MyVariant Identifiers: chrX:g.18622502C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18604382C>A , CM000685.2:g.18604382C>A	GRCh38
NC_000023.10:g.18622502C>A , CM000685.1:g.18622502C>A	GRCh37
NC_000023.9:g.18532423C>A	NCBI36
NG_008475.1:g.183778C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.1458C>A MANE Select	ENSP00000485244.1:p.Ala486=
ENST00000635828.1:c.1458C>A	ENSP00000490170.1:p.Ala486=
ENST00000674046.1:c.1458C>A	ENSP00000501174.1:p.Ala486=
ENST00000379989.6:c.1458C>A	ENSP00000369325.3:p.Ala486=
ENST00000379996.7:c.1458C>A	ENSP00000369332.3:p.Ala486=
ENST00000463994.4:c.1458C>A	ENSP00000485184.1:p.Ala486=
ENST00000623535.1:c.1458C>A	ENSP00000485244.1:p.Ala486=
NM_001037343.1:c.1458C>A	NP_001032420.1:p.Ala486=
NM_003159.2:c.1458C>A	NP_003150.1:p.Ala486=
XM_011545569.1:c.1407C>A	XP_011543871.1:p.Ala469=
XM_011545570.1:c.1326C>A	XP_011543872.1:p.Ala442=
XR_950484.1:n.1710C>A
NM_001323289.1:c.1458C>A	NP_001310218.1:p.Ala486=
NM_001323289.2:c.1458C>A MANE Select	NP_001310218.1:p.Ala486=
NM_001037343.2:c.1458C>A	NP_001032420.1:p.Ala486=
NM_003159.3:c.1458C>A	NP_003150.1:p.Ala486=