Canonical Allele Identifier: CA2693221229

Gene: CDKL5

Linked Data

• gnomAD v4: X-18575322-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18575322T>C , CM000685.2:g.18575322T>C	GRCh38
NC_000023.10:g.18593442T>C , CM000685.1:g.18593442T>C	GRCh37
NC_000023.9:g.18503363T>C	NCBI36
NG_008475.1:g.154718T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000623535.2:c.146-32T>C MANE Select	ENSP00000485244.1:n.146-32T>C
ENST00000635828.1:c.146-32T>C	ENSP00000490170.1:n.146-32T>C
ENST00000637881.1:c.146-32T>C	ENSP00000489879.1:n.146-32T>C
ENST00000674046.1:c.146-32T>C	ENSP00000501174.1:n.146-32T>C
ENST00000379989.6:c.146-32T>C	ENSP00000369325.3:n.146-32T>C
ENST00000379996.7:c.146-32T>C	ENSP00000369332.3:n.146-32T>C
ENST00000463994.4:c.146-32T>C	ENSP00000485184.1:n.146-32T>C
ENST00000623364.3:c.146-32T>C	ENSP00000485581.1:n.146-32T>C
ENST00000623535.1:c.146-32T>C	ENSP00000485244.1:n.146-32T>C
ENST00000624700.3:c.146-32T>C	ENSP00000485359.1:n.146-32T>C
NM_001037343.1:c.146-32T>C	NP_001032420.1:n.146-32T>C
NM_003159.2:c.146-32T>C	NP_003150.1:n.146-32T>C
XM_011545569.1:c.146-32T>C	XP_011543871.1:n.146-32T>C
XM_011545570.1:c.14-32T>C	XP_011543872.1:n.14-32T>C
XR_950484.1:n.398-32T>C
NM_001323289.1:c.146-32T>C	NP_001310218.1:n.146-32T>C
NM_001323289.2:c.146-32T>C MANE Select	NP_001310218.1:n.146-32T>C
NM_001037343.2:c.146-32T>C	NP_001032420.1:n.146-32T>C
NM_003159.3:c.146-32T>C	NP_003150.1:n.146-32T>C