Canonical Allele Identifier: CA10955523
Gene: KCNN3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154781718C>T , CM000663.2:g.154781718C>T GRCh38
NC_000001.10:g.154754194C>T , CM000663.1:g.154754194C>T GRCh37
NC_000001.9:g.153020818C>T NCBI36
NG_016807.2:g.93561G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271915.9:c.1030-9325G>A MANE Select ENSP00000271915.3:n.1030-9325G>A
ENST00000271915.8:c.1030-9325G>A ENSP00000271915.3:n.1030-9325G>A
ENST00000358505.2:c.91-9325G>A ENSP00000351295.2:n.91-9325G>A
ENST00000361147.8:c.115-9325G>A ENSP00000354764.4:n.115-9325G>A
ENST00000618040.4:c.1030-9325G>A ENSP00000481848.1:n.1030-9325G>A
NM_001204087.1:c.1030-9325G>A NP_001191016.1:n.1030-9325G>A
NM_002249.5:c.1030-9325G>A NP_002240.3:n.1030-9325G>A
NM_170782.2:c.115-9325G>A NP_740752.1:n.115-9325G>A
NM_001365837.1:c.91-9325G>A NP_001352766.1:n.91-9325G>A
NM_001365838.1:c.91-9325G>A NP_001352767.1:n.91-9325G>A
NM_002249.6:c.1030-9325G>A MANE Select NP_002240.3:n.1030-9325G>A
NM_170782.3:c.115-9325G>A NP_740752.1:n.115-9325G>A
NM_001204087.2:c.1030-9325G>A NP_001191016.1:n.1030-9325G>A
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