Canonical Allele Identifier: CA174965514
Gene: KCNU1 HGNC NCBI

Linked Data

dbSNP Id: rs12677095
gnomAD v2: 8-36685049-T-C
gnomAD v3: 8-36827531-T-C
gnomAD v4: 8-36827531-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.36827531T>C , CM000670.2:g.36827531T>C GRCh38
NC_000008.10:g.36685049T>C , CM000670.1:g.36685049T>C GRCh37
NC_000008.9:g.36804207T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000399881.8:c.1107-6023T>C MANE Select ENSP00000382770.3:n.1107-6023T>C
ENST00000399881.7:c.1107-6023T>C ENSP00000382770.3:n.1107-6023T>C
ENST00000522372.5:c.1107-6023T>C ENSP00000428552.1:n.1107-6023T>C
NM_001031836.2:c.1107-6023T>C NP_001027006.2:n.1107-6023T>C
XM_005273424.2:c.1107-6023T>C XP_005273481.1:n.1107-6023T>C
XM_011544423.1:c.1098-6023T>C XP_011542725.1:n.1098-6023T>C
XM_011544424.1:c.1107-6023T>C XP_011542726.1:n.1107-6023T>C
XM_011544425.1:c.1107-6023T>C XP_011542727.1:n.1107-6023T>C
XM_011544426.1:c.1107-6023T>C XP_011542728.1:n.1107-6023T>C
XM_011544427.1:c.1107-6023T>C XP_011542729.1:n.1107-6023T>C
XR_949380.1:n.1132-6023T>C
XR_949381.1:n.1132-6023T>C
XR_949382.1:n.1132-6023T>C
NR_134267.1:n.1194-6023T>C
XM_011544424.2:c.1107-6023T>C XP_011542726.1:n.1107-6023T>C
XM_011544426.2:c.1107-6023T>C XP_011542728.1:n.1107-6023T>C
XM_011544427.2:c.1107-6023T>C XP_011542729.1:n.1107-6023T>C
XM_017013144.2:c.1107-6023T>C XP_016868633.1:n.1107-6023T>C
XM_024447080.1:c.1107-6023T>C XP_024302848.1:n.1107-6023T>C
XR_001745486.2:n.1135-6023T>C
NM_001031836.3:c.1107-6023T>C MANE Select NP_001027006.2:n.1107-6023T>C
NR_134267.2:n.1144-6023T>C