Canonical Allele Identifier: CA2596406330

Gene: KCNU1

Linked Data

• gnomAD v3: 8-36827592-GCT-G
• gnomAD v4: 8-36827592-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.36827593_36827594del , CM000670.2:g.36827593_36827594del	GRCh38
NC_000008.10:g.36685111_36685112del , CM000670.1:g.36685111_36685112del	GRCh37
NC_000008.9:g.36804269_36804270del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000399881.8:c.1107-5961_1107-5960del MANE Select	ENSP00000382770.3:n.1107-5961_1107-5960de...
ENST00000399881.7:c.1107-5961_1107-5960del	ENSP00000382770.3:n.1107-5961_1107-5960de...
ENST00000522372.5:c.1107-5961_1107-5960del	ENSP00000428552.1:n.1107-5961_1107-5960de...
NM_001031836.2:c.1107-5961_1107-5960del	NP_001027006.2:n.1107-5961_1107-5960del
XM_005273424.2:c.1107-5961_1107-5960del	XP_005273481.1:n.1107-5961_1107-5960del
XM_011544423.1:c.1098-5961_1098-5960del	XP_011542725.1:n.1098-5961_1098-5960del
XM_011544424.1:c.1107-5961_1107-5960del	XP_011542726.1:n.1107-5961_1107-5960del
XM_011544425.1:c.1107-5961_1107-5960del	XP_011542727.1:n.1107-5961_1107-5960del
XM_011544426.1:c.1107-5961_1107-5960del	XP_011542728.1:n.1107-5961_1107-5960del
XM_011544427.1:c.1107-5961_1107-5960del	XP_011542729.1:n.1107-5961_1107-5960del
XR_949380.1:n.1132-5961_1132-5960del
XR_949381.1:n.1132-5961_1132-5960del
XR_949382.1:n.1132-5961_1132-5960del
NR_134267.1:n.1194-5961_1194-5960del
XM_011544424.2:c.1107-5961_1107-5960del	XP_011542726.1:n.1107-5961_1107-5960del
XM_011544426.2:c.1107-5961_1107-5960del	XP_011542728.1:n.1107-5961_1107-5960del
XM_011544427.2:c.1107-5961_1107-5960del	XP_011542729.1:n.1107-5961_1107-5960del
XM_017013144.2:c.1107-5961_1107-5960del	XP_016868633.1:n.1107-5961_1107-5960del
XM_024447080.1:c.1107-5961_1107-5960del	XP_024302848.1:n.1107-5961_1107-5960del
XR_001745486.2:n.1135-5961_1135-5960del
NM_001031836.3:c.1107-5961_1107-5960del MANE Select	NP_001027006.2:n.1107-5961_1107-5960del
NR_134267.2:n.1144-5961_1144-5960del