Canonical Allele Identifier: CA10639372
Gene: KCNE3 HGNC NCBI

Linked Data

ClinVar Variation Id: 306040
ClinVar RCV Id: RCV000395884
dbSNP Id: rs41315535
gnomAD v2: 11-74166781-G-GT
gnomAD v3: 11-74455736-G-GT
gnomAD v4: 11-74455736-G-GT
MyVariant Identifiers: chr11:g.74166782dupT (hg19) chr11:g.74166781_74166782insT (hg19) chr11:g.74455737dupT (hg38) chr11:g.74455736_74455737insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74455745dup , CM000673.2:g.74455745dup GRCh38
NC_000011.9:g.74166790dup , CM000673.1:g.74166790dup GRCh37
NC_000011.8:g.73844438dup NCBI36
NG_011833.1:g.16819dup , LRG_439:g.16819dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000310128.9:c.*1515dup MANE Select ENSP00000310557.4:n.*1515dup
ENST00000310128.8:c.*1515dup ENSP00000310557.4:n.*1515dup
NM_005472.4:c.*1515dup , LRG_439t1:c.*1515dup NP_005463.1:n.*1515dup
XM_017017047.1:c.*1515dup XP_016872536.1:n.*1515dup
XM_017017048.1:c.*1515dup XP_016872537.1:n.*1515dup
XM_017017049.1:c.*1515dup XP_016872538.1:n.*1515dup
XM_017017051.2:c.*1515dup XP_016872540.1:n.*1515dup
XM_017017052.1:c.*1515dup XP_016872541.1:n.*1515dup
NM_005472.5:c.*1515dup MANE Select NP_005463.1:n.*1515dup
Search 100 bp 5'
Search 100 bp 3'