Canonical Allele Identifier: CA10631521

Gene: KCNE3

Linked Data

• ClinVar Variation Id: 306064
• ClinVar RCV Id: RCV000304883
• dbSNP Id: rs757362085
• gnomAD v2: 11-74167386-AAG-A
• gnomAD v3: 11-74456341-AAG-A
• gnomAD v4: 11-74456341-AAG-A
• MyVariant Identifiers: chr11:g.74167387_74167388del (hg19) ; chr11:g.74456342_74456343del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74456343_74456344del , CM000673.2:g.74456343_74456344del	GRCh38
NC_000011.9:g.74167388_74167389del , CM000673.1:g.74167388_74167389del	GRCh37
NC_000011.8:g.73845036_73845037del	NCBI36
NG_011833.1:g.16213_16214del , LRG_439:g.16213_16214del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310128.9:c.*909_*910del MANE Select	ENSP00000310557.4:n.*909_*910del
ENST00000310128.8:c.*909_*910del	ENSP00000310557.4:n.*909_*910del
NM_005472.4:c.*909_*910del , LRG_439t1:c.*909_*910del	NP_005463.1:n.*909_*910del
XM_017017047.1:c.*909_*910del	XP_016872536.1:n.*909_*910del
XM_017017048.1:c.*909_*910del	XP_016872537.1:n.*909_*910del
XM_017017049.1:c.*909_*910del	XP_016872538.1:n.*909_*910del
XM_017017051.2:c.*909_*910del	XP_016872540.1:n.*909_*910del
XM_017017052.1:c.*909_*910del	XP_016872541.1:n.*909_*910del
NM_005472.5:c.*909_*910del MANE Select	NP_005463.1:n.*909_*910del