Canonical Allele Identifier: CA1131407088

Linked Data

dbSNP Id: rs1927807308
gnomAD v3: X-18647135-G-C
gnomAD v4: X-18647135-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18647135G>C , CM000685.2:g.18647135G>C GRCh38
NC_000023.10:g.18665255G>C , CM000685.1:g.18665255G>C GRCh37
NC_000023.9:g.18575176G>C NCBI36
NG_008475.1:g.226531G>C
NG_008659.3:g.35314C>G , LRG_702:g.35314C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379984.4:c.326+56C>G (RS1) MANE Select ENSP00000369320.3:n.326+56C>G
ENST00000379984.3:c.326+56C>G (RS1) ENSP00000369320.3:n.326+56C>G
ENST00000379989.6:c.2797+1045G>C (CDKL5) ENSP00000369325.3:n.2797+1045G>C
ENST00000379996.7:c.2797+1045G>C (CDKL5) ENSP00000369332.3:n.2797+1045G>C
ENST00000476595.1:n.817+56C>G (RS1)
NM_000330.3:c.326+56C>G , LRG_702t1:c.326+56C>G (RS1) NP_000321.1:n.326+56C>G
NM_001037343.1:c.2797+1045G>C (CDKL5) NP_001032420.1:n.2797+1045G>C
NM_003159.2:c.2797+1045G>C (CDKL5) NP_003150.1:n.2797+1045G>C
XM_011545569.1:c.2869+1045G>C (CDKL5) XP_011543871.1:n.2869+1045G>C
XM_011545570.1:c.2788+1045G>C (CDKL5) XP_011543872.1:n.2788+1045G>C
XR_950484.1:n.3172+1045G>C (CDKL5)
NM_000330.4:c.326+56C>G (RS1) MANE Select NP_000321.1:n.326+56C>G
NM_001037343.2:c.2797+1045G>C (CDKL5) NP_001032420.1:n.2797+1045G>C
NM_003159.3:c.2797+1045G>C (CDKL5) NP_003150.1:n.2797+1045G>C