Canonical Allele Identifier: CA2417986342

Gene: RS1 CDKL5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18641838A= , CM000685.2:g.18641838A=	GRCh38
NC_000023.10:g.18659958A= , CM000685.1:g.18659958A=	GRCh37
NC_000023.9:g.18569879A=	NCBI36
NG_008475.1:g.221234A=
NG_008659.3:g.40611T= , LRG_702:g.40611T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379984.4:c.*166T= (RS1) MANE Select	ENSP00000369320.3:n.*166T=
ENST00000379984.3:c.*166T= (RS1)	ENSP00000369320.3:n.*166T=
ENST00000379989.6:c.2714-4169A= (CDKL5)	ENSP00000369325.3:n.2714-4169A=
ENST00000379996.7:c.2714-4169A= (CDKL5)	ENSP00000369332.3:n.2714-4169A=
NM_000330.3:c.*166T= , LRG_702t1:c.*166T= (RS1)	NP_000321.1:n.*166T=
NM_001037343.1:c.2714-4169A= (CDKL5)	NP_001032420.1:n.2714-4169A=
NM_003159.2:c.2714-4169A= (CDKL5)	NP_003150.1:n.2714-4169A=
XM_011545569.1:c.2786-4169A= (CDKL5)	XP_011543871.1:n.2786-4169A=
XM_011545570.1:c.2705-4169A= (CDKL5)	XP_011543872.1:n.2705-4169A=
XR_950484.1:n.3089-4169A= (CDKL5)
NM_000330.4:c.*166T= (RS1) MANE Select	NP_000321.1:n.*166T=
NM_001037343.2:c.2714-4169A= (CDKL5)	NP_001032420.1:n.2714-4169A=
NM_003159.3:c.2714-4169A= (CDKL5)	NP_003150.1:n.2714-4169A=