Canonical Allele Identifier: CA916083841

Gene: CDKL5

Linked Data

• ClinVar Variation Id: 845526
• ClinVar RCV Id: RCV001048608
• dbSNP Id: rs1926080344

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18598513_18598517dup , CM000685.2:g.18598513_18598517dup	GRCh38
NC_000023.10:g.18616633_18616637dup , CM000685.1:g.18616633_18616637dup	GRCh37
NC_000023.9:g.18526554_18526558dup	NCBI36
NG_008475.1:g.177909_177913dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000623535.2:c.877_881dup MANE Select	ENSP00000485244.1:p.His294GlnfsTer?
ENST00000635828.1:c.877_881dup	ENSP00000490170.1:p.His294GlnfsTer?
ENST00000637881.1:c.877_881dup	ENSP00000489879.1:p.His294GlnfsTer?
ENST00000674046.1:c.877_881dup	ENSP00000501174.1:p.His294GlnfsTer?
ENST00000379989.6:c.877_881dup	ENSP00000369325.3:p.His294GlnfsTer?
ENST00000379996.7:c.877_881dup	ENSP00000369332.3:p.His294GlnfsTer?
ENST00000463994.4:c.877_881dup	ENSP00000485184.1:p.His294GlnfsTer?
ENST00000623535.1:c.877_881dup	ENSP00000485244.1:p.His294GlnfsTer?
NM_001037343.1:c.877_881dup	NP_001032420.1:p.His294GlnfsTer?
NM_003159.2:c.877_881dup	NP_003150.1:p.His294GlnfsTer?
XM_011545569.1:c.877_881dup	XP_011543871.1:p.His294GlnfsTer?
XM_011545570.1:c.745_749dup	XP_011543872.1:p.His250GlnfsTer?
XR_950484.1:n.1129_1133dup
NM_001323289.1:c.877_881dup	NP_001310218.1:p.His294GlnfsTer?
NM_001323289.2:c.877_881dup MANE Select	NP_001310218.1:p.His294GlnfsTer?
NM_001037343.2:c.877_881dup	NP_001032420.1:p.His294GlnfsTer?
NM_003159.3:c.877_881dup	NP_003150.1:p.His294GlnfsTer?