Canonical Allele Identifier: CA2838206513
Gene: KCNN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154772107del , CM000663.2:g.154772107del GRCh38
NC_000001.10:g.154744583del , CM000663.1:g.154744583del GRCh37
NC_000001.9:g.153011207del NCBI36
NG_016807.2:g.103174del

Transcript Alleles

HGVS Amino-acid Change
ENST00000271915.9:c.1318del MANE Select ENSP00000271915.3:p.Leu440SerfsTer12
ENST00000271915.8:c.1318del ENSP00000271915.3:p.Leu440SerfsTer12
ENST00000358505.2:c.379del ENSP00000351295.2:p.Leu127SerfsTer12
ENST00000361147.8:c.403del ENSP00000354764.4:p.Leu135SerfsTer12
ENST00000618040.4:c.1318del ENSP00000481848.1:p.Leu440SerfsTer12
NM_001204087.1:c.1318del NP_001191016.1:p.Leu440SerfsTer12
NM_002249.5:c.1318del NP_002240.3:p.Leu440SerfsTer12
NM_170782.2:c.403del NP_740752.1:p.Leu135SerfsTer12
NM_001365837.1:c.379del NP_001352766.1:p.Leu127SerfsTer12
NM_001365838.1:c.379del NP_001352767.1:p.Leu127SerfsTer12
NM_002249.6:c.1318del MANE Select NP_002240.3:p.Leu440SerfsTer12
NM_170782.3:c.403del NP_740752.1:p.Leu135SerfsTer12
NM_001204087.2:c.1318del NP_001191016.1:p.Leu440SerfsTer12