Canonical Allele Identifier: CA2573158476

Gene: CDKL5

Linked Data

• ClinVar Variation Id: 1400702
• ClinVar RCV Id: RCV001896737
• dbSNP Id: rs2147161299

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18604820del , CM000685.2:g.18604820del	GRCh38
NC_000023.10:g.18622940del , CM000685.1:g.18622940del	GRCh37
NC_000023.9:g.18532861del	NCBI36
NG_008475.1:g.184216del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.1896del MANE Select	ENSP00000485244.1:p.Gln633LysfsTer25
ENST00000635828.1:c.1896del	ENSP00000490170.1:p.Gln633LysfsTer25
ENST00000674046.1:c.1896del	ENSP00000501174.1:p.Gln633LysfsTer25
ENST00000379989.6:c.1896del	ENSP00000369325.3:p.Gln633LysfsTer25
ENST00000379996.7:c.1896del	ENSP00000369332.3:p.Gln633LysfsTer25
ENST00000463994.4:c.1896del	ENSP00000485184.1:p.Gln633LysfsTer25
ENST00000623535.1:c.1896del	ENSP00000485244.1:p.Gln633LysfsTer25
NM_001037343.1:c.1896del	NP_001032420.1:p.Gln633LysfsTer25
NM_003159.2:c.1896del	NP_003150.1:p.Gln633LysfsTer25
XM_011545569.1:c.1845del	XP_011543871.1:p.Gln616LysfsTer25
XM_011545570.1:c.1764del	XP_011543872.1:p.Gln589LysfsTer25
XR_950484.1:n.2148del
NM_001323289.1:c.1896del	NP_001310218.1:p.Gln633LysfsTer25
NM_001323289.2:c.1896del MANE Select	NP_001310218.1:p.Gln633LysfsTer25
NM_001037343.2:c.1896del	NP_001032420.1:p.Gln633LysfsTer25
NM_003159.3:c.1896del	NP_003150.1:p.Gln633LysfsTer25