Canonical Allele Identifier: CA412367132

Gene: CDKL5

Linked Data

• MyVariant Identifiers: chrX:g.18646537C>A (hg19) ; chrX:g.18628417C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18628417C>A , CM000685.2:g.18628417C>A	GRCh38
NC_000023.10:g.18646537C>A , CM000685.1:g.18646537C>A	GRCh37
NC_000023.9:g.18556458C>A	NCBI36
NG_008475.1:g.207813C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.2543C>A MANE Select	ENSP00000485244.1:p.Ala848Asp
ENST00000674046.1:c.2666C>A	ENSP00000501174.1:p.Ala889Asp
ENST00000379989.6:c.2543C>A	ENSP00000369325.3:p.Ala848Asp
ENST00000379996.7:c.2543C>A	ENSP00000369332.3:p.Ala848Asp
ENST00000623535.1:c.2543C>A	ENSP00000485244.1:p.Ala848Asp
NM_001037343.1:c.2543C>A	NP_001032420.1:p.Ala848Asp
NM_003159.2:c.2543C>A	NP_003150.1:p.Ala848Asp
XM_011545569.1:c.2615C>A	XP_011543871.1:p.Ala872Asp
XM_011545570.1:c.2534C>A	XP_011543872.1:p.Ala845Asp
XR_950484.1:n.2918C>A
NM_001323289.1:c.2543C>A	NP_001310218.1:p.Ala848Asp
NM_001323289.2:c.2543C>A MANE Select	NP_001310218.1:p.Ala848Asp
NM_001037343.2:c.2543C>A	NP_001032420.1:p.Ala848Asp
NM_003159.3:c.2543C>A	NP_003150.1:p.Ala848Asp