Canonical Allele Identifier: CA412362191

Gene: CDKL5

Linked Data

• ClinVar Variation Id: 1479406
• ClinVar RCV Id: RCV001990942
• dbSNP Id: rs2147160978
• MyVariant Identifiers: chrX:g.18622711A>G (hg19) ; chrX:g.18604591A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18604591A>G , CM000685.2:g.18604591A>G	GRCh38
NC_000023.10:g.18622711A>G , CM000685.1:g.18622711A>G	GRCh37
NC_000023.9:g.18532632A>G	NCBI36
NG_008475.1:g.183987A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.1667A>G MANE Select	ENSP00000485244.1:p.Asp556Gly
ENST00000635828.1:c.1667A>G	ENSP00000490170.1:p.Asp556Gly
ENST00000674046.1:c.1667A>G	ENSP00000501174.1:p.Asp556Gly
ENST00000379989.6:c.1667A>G	ENSP00000369325.3:p.Asp556Gly
ENST00000379996.7:c.1667A>G	ENSP00000369332.3:p.Asp556Gly
ENST00000463994.4:c.1667A>G	ENSP00000485184.1:p.Asp556Gly
ENST00000623535.1:c.1667A>G	ENSP00000485244.1:p.Asp556Gly
NM_001037343.1:c.1667A>G	NP_001032420.1:p.Asp556Gly
NM_003159.2:c.1667A>G	NP_003150.1:p.Asp556Gly
XM_011545569.1:c.1616A>G	XP_011543871.1:p.Asp539Gly
XM_011545570.1:c.1535A>G	XP_011543872.1:p.Asp512Gly
XR_950484.1:n.1919A>G
NM_001323289.1:c.1667A>G	NP_001310218.1:p.Asp556Gly
NM_001323289.2:c.1667A>G MANE Select	NP_001310218.1:p.Asp556Gly
NM_001037343.2:c.1667A>G	NP_001032420.1:p.Asp556Gly
NM_003159.3:c.1667A>G	NP_003150.1:p.Asp556Gly