Canonical Allele Identifier: CA1140442008

Gene: KCNN3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154841877C= , CM000663.2:g.154841877C=	GRCh38
NC_000001.10:g.154814353C= , CM000663.1:g.154814353C=	GRCh37
NC_000001.9:g.153080977C=	NCBI36
NG_016807.2:g.33402G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271915.9:c.934-19693G= MANE Select	ENSP00000271915.3:n.934-19693G=
ENST00000271915.8:c.934-19693G=	ENSP00000271915.3:n.934-19693G=
ENST00000358505.2:c.-6-19693G=	ENSP00000351295.2:n.-6-19693G=
ENST00000361147.8:c.18+17818G=	ENSP00000354764.4:n.18+17818G=
ENST00000618040.4:c.934-19693G=	ENSP00000481848.1:n.934-19693G=
NM_001204087.1:c.934-19693G=	NP_001191016.1:n.934-19693G=
NM_002249.5:c.934-19693G=	NP_002240.3:n.934-19693G=
NM_170782.2:c.18+17818G=	NP_740752.1:n.18+17818G=
NM_001365837.1:c.-6-19693G=	NP_001352766.1:n.-6-19693G=
NM_001365838.1:c.-6-19693G=	NP_001352767.1:n.-6-19693G=
NM_002249.6:c.934-19693G= MANE Select	NP_002240.3:n.934-19693G=
NM_170782.3:c.18+17818G=	NP_740752.1:n.18+17818G=
NM_001204087.2:c.934-19693G=	NP_001191016.1:n.934-19693G=