Canonical Allele Identifier: CA412367571

Gene: CDKL5

Linked Data

• MyVariant Identifiers: chrX:g.18646621T>C (hg19) ; chrX:g.18628501T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18628501T>C , CM000685.2:g.18628501T>C	GRCh38
NC_000023.10:g.18646621T>C , CM000685.1:g.18646621T>C	GRCh37
NC_000023.9:g.18556542T>C	NCBI36
NG_008475.1:g.207897T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623535.2:c.2627T>C MANE Select	ENSP00000485244.1:p.Ile876Thr
ENST00000674046.1:c.2750T>C	ENSP00000501174.1:p.Ile917Thr
ENST00000379989.6:c.2627T>C	ENSP00000369325.3:p.Ile876Thr
ENST00000379996.7:c.2627T>C	ENSP00000369332.3:p.Ile876Thr
ENST00000623535.1:c.2627T>C	ENSP00000485244.1:p.Ile876Thr
NM_001037343.1:c.2627T>C	NP_001032420.1:p.Ile876Thr
NM_003159.2:c.2627T>C	NP_003150.1:p.Ile876Thr
XM_011545569.1:c.2699T>C	XP_011543871.1:p.Ile900Thr
XM_011545570.1:c.2618T>C	XP_011543872.1:p.Ile873Thr
XR_950484.1:n.3002T>C
NM_001323289.1:c.2627T>C	NP_001310218.1:p.Ile876Thr
NM_001323289.2:c.2627T>C MANE Select	NP_001310218.1:p.Ile876Thr
NM_001037343.2:c.2627T>C	NP_001032420.1:p.Ile876Thr
NM_003159.3:c.2627T>C	NP_003150.1:p.Ile876Thr