Canonical Allele Identifier: CA412372427

Gene: RS1 CDKL5

Linked Data

• MyVariant Identifiers: chrX:g.18664152G>T (hg19) ; chrX:g.18646032G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18646032G>T , CM000685.2:g.18646032G>T	GRCh38
NC_000023.10:g.18664152G>T , CM000685.1:g.18664152G>T	GRCh37
NC_000023.9:g.18574073G>T	NCBI36
NG_008475.1:g.225428G>T
NG_008659.3:g.36417C>A , LRG_702:g.36417C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379984.4:c.326+1159C>A (RS1) MANE Select	ENSP00000369320.3:n.326+1159C>A
ENST00000379984.3:c.326+1159C>A (RS1)	ENSP00000369320.3:n.326+1159C>A
ENST00000379989.6:c.2739G>T (CDKL5)	ENSP00000369325.3:p.Gln913His
ENST00000379996.7:c.2739G>T (CDKL5)	ENSP00000369332.3:p.Gln913His
ENST00000476595.1:n.817+1159C>A (RS1)
NM_000330.3:c.326+1159C>A , LRG_702t1:c.326+1159C>A (RS1)	NP_000321.1:n.326+1159C>A
NM_001037343.1:c.2739G>T (CDKL5)	NP_001032420.1:p.Gln913His
NM_003159.2:c.2739G>T (CDKL5)	NP_003150.1:p.Gln913His
XM_011545569.1:c.2811G>T (CDKL5)	XP_011543871.1:p.Gln937His
XM_011545570.1:c.2730G>T (CDKL5)	XP_011543872.1:p.Gln910His
XR_950484.1:n.3114G>T (CDKL5)
NM_000330.4:c.326+1159C>A (RS1) MANE Select	NP_000321.1:n.326+1159C>A
NM_001037343.2:c.2739G>T (CDKL5)	NP_001032420.1:p.Gln913His
NM_003159.3:c.2739G>T (CDKL5)	NP_003150.1:p.Gln913His