Canonical Allele Identifier: CA10639403
Gene: KCNE3 HGNC NCBI

Linked Data

ClinVar Variation Id: 306062
ClinVar RCV Id: RCV000340003
dbSNP Id: rs60016728
gnomAD v2: 11-74167374-C-CAAA
gnomAD v3: 11-74456329-C-CAAA
gnomAD v4: 11-74456329-C-CAAA
MyVariant Identifiers: chr11:g.74167375_74167377dupAAA (hg19) chr11:g.74167387_74167388insAAA (hg19) chr11:g.74167375_74167376insAAA (hg19) chr11:g.74167374_74167375insAAA (hg19) chr11:g.74456330_74456332dupAAA (hg38) chr11:g.74456342_74456343insAAA (hg38) chr11:g.74456330_74456331insAAA (hg38) chr11:g.74456329_74456330insAAA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74456340_74456342dup , CM000673.2:g.74456340_74456342dup GRCh38
NC_000011.9:g.74167385_74167387dup , CM000673.1:g.74167385_74167387dup GRCh37
NC_000011.8:g.73845033_73845035dup NCBI36
NG_011833.1:g.16224_16226dup , LRG_439:g.16224_16226dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000310128.9:c.*920_*922dup MANE Select ENSP00000310557.4:n.*920_*922dup
ENST00000310128.8:c.*920_*922dup ENSP00000310557.4:n.*920_*922dup
NM_005472.4:c.*920_*922dup , LRG_439t1:c.*920_*922dup NP_005463.1:n.*920_*922dup
XM_017017047.1:c.*920_*922dup XP_016872536.1:n.*920_*922dup
XM_017017048.1:c.*920_*922dup XP_016872537.1:n.*920_*922dup
XM_017017049.1:c.*920_*922dup XP_016872538.1:n.*920_*922dup
XM_017017051.2:c.*920_*922dup XP_016872540.1:n.*920_*922dup
XM_017017052.1:c.*920_*922dup XP_016872541.1:n.*920_*922dup
NM_005472.5:c.*920_*922dup MANE Select NP_005463.1:n.*920_*922dup
Search 100 bp 5'
Search 100 bp 3'