Canonical Allele Identifier: CA2417974316
Gene: CDKL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18603835T= , CM000685.2:g.18603835T= GRCh38
NC_000023.10:g.18621955T= , CM000685.1:g.18621955T= GRCh37
NC_000023.9:g.18531876T= NCBI36
NG_008475.1:g.183231T=

Transcript Alleles

HGVS Amino-acid change
ENST00000623535.2:c.978-67T= MANE Select ENSP00000485244.1:n.978-67T=
ENST00000635828.1:c.978-67T= ENSP00000490170.1:n.978-67T=
ENST00000637881.1:c.978-67T= ENSP00000489879.1:n.978-67T=
ENST00000674046.1:c.978-67T= ENSP00000501174.1:n.978-67T=
ENST00000379989.6:c.978-67T= ENSP00000369325.3:n.978-67T=
ENST00000379996.7:c.978-67T= ENSP00000369332.3:n.978-67T=
ENST00000463994.4:c.978-67T= ENSP00000485184.1:n.978-67T=
ENST00000623535.1:c.978-67T= ENSP00000485244.1:n.978-67T=
NM_001037343.1:c.978-67T= NP_001032420.1:n.978-67T=
NM_003159.2:c.978-67T= NP_003150.1:n.978-67T=
XM_011545569.1:c.927-67T= XP_011543871.1:n.927-67T=
XM_011545570.1:c.846-67T= XP_011543872.1:n.846-67T=
XR_950484.1:n.1230-67T=
NM_001323289.1:c.978-67T= NP_001310218.1:n.978-67T=
NM_001323289.2:c.978-67T= MANE Select NP_001310218.1:n.978-67T=
NM_001037343.2:c.978-67T= NP_001032420.1:n.978-67T=
NM_003159.3:c.978-67T= NP_003150.1:n.978-67T=