Canonical Allele Identifier: CA1139887249

Gene: KCNN3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154804681G= , CM000663.2:g.154804681G=	GRCh38
NC_000001.10:g.154777157G= , CM000663.1:g.154777157G=	GRCh37
NC_000001.9:g.153043781G=	NCBI36
NG_016807.2:g.70598C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271915.9:c.1029+17408C= MANE Select	ENSP00000271915.3:n.1029+17408C=
ENST00000271915.8:c.1029+17408C=	ENSP00000271915.3:n.1029+17408C=
ENST00000358505.2:c.90+17408C=	ENSP00000351295.2:n.90+17408C=
ENST00000361147.8:c.114+17408C=	ENSP00000354764.4:n.114+17408C=
ENST00000618040.4:c.1029+17408C=	ENSP00000481848.1:n.1029+17408C=
NM_001204087.1:c.1029+17408C=	NP_001191016.1:n.1029+17408C=
NM_002249.5:c.1029+17408C=	NP_002240.3:n.1029+17408C=
NM_170782.2:c.114+17408C=	NP_740752.1:n.114+17408C=
NM_001365837.1:c.90+17408C=	NP_001352766.1:n.90+17408C=
NM_001365838.1:c.90+17408C=	NP_001352767.1:n.90+17408C=
NM_002249.6:c.1029+17408C= MANE Select	NP_002240.3:n.1029+17408C=
NM_170782.3:c.114+17408C=	NP_740752.1:n.114+17408C=
NM_001204087.2:c.1029+17408C=	NP_001191016.1:n.1029+17408C=