Canonical Allele Identifier: CA1139853293

Gene: KCNN3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154772376A= , CM000663.2:g.154772376A=	GRCh38
NC_000001.10:g.154744852A= , CM000663.1:g.154744852A=	GRCh37
NC_000001.9:g.153011476A=	NCBI36
NG_016807.2:g.102903T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271915.9:c.1047T= MANE Select	ENSP00000271915.3:p.Asn349=
ENST00000271915.8:c.1047T=	ENSP00000271915.3:p.Asn349=
ENST00000358505.2:c.108T=	ENSP00000351295.2:p.Asn36=
ENST00000361147.8:c.132T=	ENSP00000354764.4:p.Asn44=
ENST00000618040.4:c.1047T=	ENSP00000481848.1:p.Asn349=
NM_001204087.1:c.1047T=	NP_001191016.1:p.Asn349=
NM_002249.5:c.1047T=	NP_002240.3:p.Asn349=
NM_170782.2:c.132T=	NP_740752.1:p.Asn44=
NM_001365837.1:c.108T=	NP_001352766.1:p.Asn36=
NM_001365838.1:c.108T=	NP_001352767.1:p.Asn36=
NM_002249.6:c.1047T= MANE Select	NP_002240.3:p.Asn349=
NM_170782.3:c.132T=	NP_740752.1:p.Asn44=
NM_001204087.2:c.1047T=	NP_001191016.1:p.Asn349=