Canonical Allele Identifier: CA343065934

Gene: KCNN3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154708065C>A , CM000663.2:g.154708065C>A	GRCh38
NC_000001.10:g.154680541C>A , CM000663.1:g.154680541C>A	GRCh37
NC_000001.9:g.152947165C>A	NCBI36
NG_016807.2:g.167214G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271915.9:c.2107G>T MANE Select	ENSP00000271915.3:p.Gly703Cys
ENST00000271915.8:c.2107G>T	ENSP00000271915.3:p.Gly703Cys
ENST00000358505.2:c.1168G>T	ENSP00000351295.2:p.Gly390Cys
ENST00000361147.8:c.1192G>T	ENSP00000354764.4:p.Gly398Cys
ENST00000515643.1:n.162G>T
ENST00000618040.4:c.2152G>T	ENSP00000481848.1:p.Gly718Cys
NM_001204087.1:c.2152G>T	NP_001191016.1:p.Gly718Cys
NM_002249.5:c.2107G>T	NP_002240.3:p.Gly703Cys
NM_170782.2:c.1192G>T	NP_740752.1:p.Gly398Cys
NM_001365837.1:c.1213G>T	NP_001352766.1:p.Gly405Cys
NM_001365838.1:c.1168G>T	NP_001352767.1:p.Gly390Cys
NM_002249.6:c.2107G>T MANE Select	NP_002240.3:p.Gly703Cys
NM_170782.3:c.1192G>T	NP_740752.1:p.Gly398Cys
NM_001204087.2:c.2152G>T	NP_001191016.1:p.Gly718Cys