Canonical Allele Identifier: CA1131402214

Gene: CDKL5

Linked Data

• dbSNP Id: rs1927131044
• gnomAD v3: X-18628319-CT-C
• gnomAD v4: X-18628319-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18628321del , CM000685.2:g.18628321del	GRCh38
NC_000023.10:g.18646441del , CM000685.1:g.18646441del	GRCh37
NC_000023.9:g.18556362del	NCBI36
NG_008475.1:g.207717del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.2497-50del MANE Select	ENSP00000485244.1:n.2497-50del
ENST00000674046.1:c.2620-50del	ENSP00000501174.1:n.2620-50del
ENST00000379989.6:c.2497-50del	ENSP00000369325.3:n.2497-50del
ENST00000379996.7:c.2497-50del	ENSP00000369332.3:n.2497-50del
ENST00000623535.1:c.2497-50del	ENSP00000485244.1:n.2497-50del
NM_001037343.1:c.2497-50del	NP_001032420.1:n.2497-50del
NM_003159.2:c.2497-50del	NP_003150.1:n.2497-50del
XM_011545569.1:c.2569-50del	XP_011543871.1:n.2569-50del
XM_011545570.1:c.2488-50del	XP_011543872.1:n.2488-50del
XR_950484.1:n.2872-50del
NM_001323289.1:c.2497-50del	NP_001310218.1:n.2497-50del
NM_001323289.2:c.2497-50del MANE Select	NP_001310218.1:n.2497-50del
NM_001037343.2:c.2497-50del	NP_001032420.1:n.2497-50del
NM_003159.3:c.2497-50del	NP_003150.1:n.2497-50del