Canonical Allele Identifier: CA1112787815
Gene: KCNU1 HGNC NCBI

Linked Data

dbSNP Id: rs1804369408

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.36827498_36827499del , CM000670.2:g.36827498_36827499del GRCh38
NC_000008.10:g.36685016_36685017del , CM000670.1:g.36685016_36685017del GRCh37
NC_000008.9:g.36804174_36804175del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000399881.8:c.1107-6056_1107-6055del MANE Select ENSP00000382770.3:n.1107-6056_1107-6055del
ENST00000399881.7:c.1107-6056_1107-6055del ENSP00000382770.3:n.1107-6056_1107-6055del
ENST00000522372.5:c.1107-6056_1107-6055del ENSP00000428552.1:n.1107-6056_1107-6055del
NM_001031836.2:c.1107-6056_1107-6055del NP_001027006.2:n.1107-6056_1107-6055del
XM_005273424.2:c.1107-6056_1107-6055del XP_005273481.1:n.1107-6056_1107-6055del
XM_011544423.1:c.1098-6056_1098-6055del XP_011542725.1:n.1098-6056_1098-6055del
XM_011544424.1:c.1107-6056_1107-6055del XP_011542726.1:n.1107-6056_1107-6055del
XM_011544425.1:c.1107-6056_1107-6055del XP_011542727.1:n.1107-6056_1107-6055del
XM_011544426.1:c.1107-6056_1107-6055del XP_011542728.1:n.1107-6056_1107-6055del
XM_011544427.1:c.1107-6056_1107-6055del XP_011542729.1:n.1107-6056_1107-6055del
XR_949380.1:n.1132-6056_1132-6055del
XR_949381.1:n.1132-6056_1132-6055del
XR_949382.1:n.1132-6056_1132-6055del
NR_134267.1:n.1194-6056_1194-6055del
XM_011544424.2:c.1107-6056_1107-6055del XP_011542726.1:n.1107-6056_1107-6055del
XM_011544426.2:c.1107-6056_1107-6055del XP_011542728.1:n.1107-6056_1107-6055del
XM_011544427.2:c.1107-6056_1107-6055del XP_011542729.1:n.1107-6056_1107-6055del
XM_017013144.2:c.1107-6056_1107-6055del XP_016868633.1:n.1107-6056_1107-6055del
XM_024447080.1:c.1107-6056_1107-6055del XP_024302848.1:n.1107-6056_1107-6055del
XR_001745486.2:n.1135-6056_1135-6055del
NM_001031836.3:c.1107-6056_1107-6055del MANE Select NP_001027006.2:n.1107-6056_1107-6055del
NR_134267.2:n.1144-6056_1144-6055del