Canonical Allele Identifier: CA889640206

Gene: KCNN3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154778513G>C , CM000663.2:g.154778513G>C	GRCh38
NC_000001.10:g.154750989G>C , CM000663.1:g.154750989G>C	GRCh37
NC_000001.9:g.153017613G>C	NCBI36
NG_016807.2:g.96766C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271915.9:c.1030-6120C>G MANE Select	ENSP00000271915.3:n.1030-6120C>G
ENST00000271915.8:c.1030-6120C>G	ENSP00000271915.3:n.1030-6120C>G
ENST00000358505.2:c.91-6120C>G	ENSP00000351295.2:n.91-6120C>G
ENST00000361147.8:c.115-6120C>G	ENSP00000354764.4:n.115-6120C>G
ENST00000618040.4:c.1030-6120C>G	ENSP00000481848.1:n.1030-6120C>G
NM_001204087.1:c.1030-6120C>G	NP_001191016.1:n.1030-6120C>G
NM_002249.5:c.1030-6120C>G	NP_002240.3:n.1030-6120C>G
NM_170782.2:c.115-6120C>G	NP_740752.1:n.115-6120C>G
NM_001365837.1:c.91-6120C>G	NP_001352766.1:n.91-6120C>G
NM_001365838.1:c.91-6120C>G	NP_001352767.1:n.91-6120C>G
NM_002249.6:c.1030-6120C>G MANE Select	NP_002240.3:n.1030-6120C>G
NM_170782.3:c.115-6120C>G	NP_740752.1:n.115-6120C>G
NM_001204087.2:c.1030-6120C>G	NP_001191016.1:n.1030-6120C>G