Canonical Allele Identifier: CA343067385

Gene: KCNN3

Linked Data

• MyVariant Identifiers: chr1:g.154744865A>T (hg19) ; chr1:g.154772389A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154772389A>T , CM000663.2:g.154772389A>T	GRCh38
NC_000001.10:g.154744865A>T , CM000663.1:g.154744865A>T	GRCh37
NC_000001.9:g.153011489A>T	NCBI36
NG_016807.2:g.102890T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000271915.9:c.1034T>A MANE Select	ENSP00000271915.3:p.Phe345Tyr
ENST00000271915.8:c.1034T>A	ENSP00000271915.3:p.Phe345Tyr
ENST00000358505.2:c.95T>A	ENSP00000351295.2:p.Phe32Tyr
ENST00000361147.8:c.119T>A	ENSP00000354764.4:p.Phe40Tyr
ENST00000618040.4:c.1034T>A	ENSP00000481848.1:p.Phe345Tyr
NM_001204087.1:c.1034T>A	NP_001191016.1:p.Phe345Tyr
NM_002249.5:c.1034T>A	NP_002240.3:p.Phe345Tyr
NM_170782.2:c.119T>A	NP_740752.1:p.Phe40Tyr
NM_001365837.1:c.95T>A	NP_001352766.1:p.Phe32Tyr
NM_001365838.1:c.95T>A	NP_001352767.1:p.Phe32Tyr
NM_002249.6:c.1034T>A MANE Select	NP_002240.3:p.Phe345Tyr
NM_170782.3:c.119T>A	NP_740752.1:p.Phe40Tyr
NM_001204087.2:c.1034T>A	NP_001191016.1:p.Phe345Tyr