Canonical Allele Identifier: CA2580617640

Gene: CDKL5

Linked Data

• ClinVar Variation Id: 2578431
• ClinVar RCV Id: RCV003326207

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18584329_18584334del , CM000685.2:g.18584329_18584334del	GRCh38
NC_000023.10:g.18602449_18602454del , CM000685.1:g.18602449_18602454del	GRCh37
NC_000023.9:g.18512370_18512375del	NCBI36
NG_008475.1:g.163725_163730del

Transcript Alleles

HGVS	Amino-acid change
ENST00000623535.2:c.530_535del MANE Select	ENSP00000485244.1:p.Tyr177_Arg178del
ENST00000635828.1:c.530_535del	ENSP00000490170.1:p.Tyr177_Arg178del
ENST00000637881.1:c.530_535del	ENSP00000489879.1:p.Tyr177_Arg178del
ENST00000674046.1:c.530_535del	ENSP00000501174.1:p.Tyr177_Arg178del
ENST00000379989.6:c.530_535del	ENSP00000369325.3:p.Tyr177_Arg178del
ENST00000379996.7:c.530_535del	ENSP00000369332.3:p.Tyr177_Arg178del
ENST00000463994.4:c.530_535del	ENSP00000485184.1:p.Tyr177_Arg178del
ENST00000623535.1:c.530_535del	ENSP00000485244.1:p.Tyr177_Arg178del
NM_001037343.1:c.530_535del	NP_001032420.1:p.Tyr177_Arg178del
NM_003159.2:c.530_535del	NP_003150.1:p.Tyr177_Arg178del
XM_011545569.1:c.530_535del	XP_011543871.1:p.Tyr177_Arg178del
XM_011545570.1:c.398_403del	XP_011543872.1:p.Tyr133_Arg134del
XR_950484.1:n.782_787del
NM_001323289.1:c.530_535del	NP_001310218.1:p.Tyr177_Arg178del
NM_001323289.2:c.530_535del MANE Select	NP_001310218.1:p.Tyr177_Arg178del
NM_001037343.2:c.530_535del	NP_001032420.1:p.Tyr177_Arg178del
NM_003159.3:c.530_535del	NP_003150.1:p.Tyr177_Arg178del