Canonical Allele Identifier: CA2417988265

Gene: RS1 CDKL5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18647296C= , CM000685.2:g.18647296C=	GRCh38
NC_000023.10:g.18665416C= , CM000685.1:g.18665416C=	GRCh37
NC_000023.9:g.18575337C=	NCBI36
NG_008475.1:g.226692C=
NG_008659.3:g.35153G= , LRG_702:g.35153G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000330.4:c.221G= (RS1) MANE Select	NP_000321.1:p.Gly74=
ENST00000379984.4:c.221G= (RS1) MANE Select	ENSP00000369320.3:p.Gly74=
NM_000330.3:c.221G= , LRG_702t1:c.221G= (RS1)	NP_000321.1:p.Gly74=
NM_001037343.1:c.2797+1206C= (CDKL5)	NP_001032420.1:n.2797+1206C=
NM_001037343.2:c.2797+1206C= (CDKL5)	NP_001032420.1:n.2797+1206C=
NM_003159.2:c.2797+1206C= (CDKL5)	NP_003150.1:n.2797+1206C=
NM_003159.3:c.2797+1206C= (CDKL5)	NP_003150.1:n.2797+1206C=
ENST00000379984.3:c.221G= (RS1)	ENSP00000369320.3:p.Gly74=
ENST00000379989.6:c.2797+1206C= (CDKL5)	ENSP00000369325.3:n.2797+1206C=
ENST00000379996.7:c.2797+1206C= (CDKL5)	ENSP00000369332.3:n.2797+1206C=
ENST00000476595.1:n.712G= (RS1)
XM_011545569.1:c.2869+1206C= (CDKL5)	XP_011543871.1:n.2869+1206C=
XM_011545570.1:c.2788+1206C= (CDKL5)	XP_011543872.1:n.2788+1206C=
XR_950484.1:n.3172+1206C= (CDKL5)