Canonical Allele Identifier: CA10687724

Gene: KCNN3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154841792G>C , CM000663.2:g.154841792G>C	GRCh38
NC_000001.10:g.154814268G>C , CM000663.1:g.154814268G>C	GRCh37
NC_000001.9:g.153080892G>C	NCBI36
NG_016807.2:g.33487C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002249.6:c.934-19608C>G MANE Select	NP_002240.3:n.934-19608C>G
ENST00000271915.9:c.934-19608C>G MANE Select	ENSP00000271915.3:n.934-19608C>G
NM_001204087.1:c.934-19608C>G	NP_001191016.1:n.934-19608C>G
NM_001204087.2:c.934-19608C>G	NP_001191016.1:n.934-19608C>G
NM_001365837.1:c.-6-19608C>G	NP_001352766.1:n.-6-19608C>G
NM_001365838.1:c.-6-19608C>G	NP_001352767.1:n.-6-19608C>G
NM_002249.5:c.934-19608C>G	NP_002240.3:n.934-19608C>G
NM_170782.2:c.18+17903C>G	NP_740752.1:n.18+17903C>G
NM_170782.3:c.18+17903C>G	NP_740752.1:n.18+17903C>G
ENST00000271915.8:c.934-19608C>G	ENSP00000271915.3:n.934-19608C>G
ENST00000358505.2:c.-6-19608C>G	ENSP00000351295.2:n.-6-19608C>G
ENST00000361147.8:c.18+17903C>G	ENSP00000354764.4:n.18+17903C>G
ENST00000618040.4:c.934-19608C>G	ENSP00000481848.1:n.934-19608C>G