Canonical Allele Identifier: CA174965458

Gene: KCNU1

Linked Data

• dbSNP Id: rs1043132306
• gnomAD v2: 8-36684981-C-T
• gnomAD v3: 8-36827463-C-T
• gnomAD v4: 8-36827463-C-T
• MyVariant Identifiers: chr8:g.36684981C>T (hg19) ; chr8:g.36827463C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.36827463C>T , CM000670.2:g.36827463C>T	GRCh38
NC_000008.10:g.36684981C>T , CM000670.1:g.36684981C>T	GRCh37
NC_000008.9:g.36804139C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000399881.8:c.1107-6091C>T MANE Select	ENSP00000382770.3:n.1107-6091C>T
ENST00000399881.7:c.1107-6091C>T	ENSP00000382770.3:n.1107-6091C>T
ENST00000522372.5:c.1107-6091C>T	ENSP00000428552.1:n.1107-6091C>T
NM_001031836.2:c.1107-6091C>T	NP_001027006.2:n.1107-6091C>T
XM_005273424.2:c.1107-6091C>T	XP_005273481.1:n.1107-6091C>T
XM_011544423.1:c.1098-6091C>T	XP_011542725.1:n.1098-6091C>T
XM_011544424.1:c.1107-6091C>T	XP_011542726.1:n.1107-6091C>T
XM_011544425.1:c.1107-6091C>T	XP_011542727.1:n.1107-6091C>T
XM_011544426.1:c.1107-6091C>T	XP_011542728.1:n.1107-6091C>T
XM_011544427.1:c.1107-6091C>T	XP_011542729.1:n.1107-6091C>T
XR_949380.1:n.1132-6091C>T
XR_949381.1:n.1132-6091C>T
XR_949382.1:n.1132-6091C>T
NR_134267.1:n.1194-6091C>T
XM_011544424.2:c.1107-6091C>T	XP_011542726.1:n.1107-6091C>T
XM_011544426.2:c.1107-6091C>T	XP_011542728.1:n.1107-6091C>T
XM_011544427.2:c.1107-6091C>T	XP_011542729.1:n.1107-6091C>T
XM_017013144.2:c.1107-6091C>T	XP_016868633.1:n.1107-6091C>T
XM_024447080.1:c.1107-6091C>T	XP_024302848.1:n.1107-6091C>T
XR_001745486.2:n.1135-6091C>T
NM_001031836.3:c.1107-6091C>T MANE Select	NP_001027006.2:n.1107-6091C>T
NR_134267.2:n.1144-6091C>T