Canonical Allele Identifier: CA343067365

Gene: KCNN3

Linked Data

• MyVariant Identifiers: chr1:g.154744857C>A (hg19) ; chr1:g.154772381C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154772381C>A , CM000663.2:g.154772381C>A	GRCh38
NC_000001.10:g.154744857C>A , CM000663.1:g.154744857C>A	GRCh37
NC_000001.9:g.153011481C>A	NCBI36
NG_016807.2:g.102898G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000271915.9:c.1042G>T MANE Select	ENSP00000271915.3:p.Asp348Tyr
ENST00000271915.8:c.1042G>T	ENSP00000271915.3:p.Asp348Tyr
ENST00000358505.2:c.103G>T	ENSP00000351295.2:p.Asp35Tyr
ENST00000361147.8:c.127G>T	ENSP00000354764.4:p.Asp43Tyr
ENST00000618040.4:c.1042G>T	ENSP00000481848.1:p.Asp348Tyr
NM_001204087.1:c.1042G>T	NP_001191016.1:p.Asp348Tyr
NM_002249.5:c.1042G>T	NP_002240.3:p.Asp348Tyr
NM_170782.2:c.127G>T	NP_740752.1:p.Asp43Tyr
NM_001365837.1:c.103G>T	NP_001352766.1:p.Asp35Tyr
NM_001365838.1:c.103G>T	NP_001352767.1:p.Asp35Tyr
NM_002249.6:c.1042G>T MANE Select	NP_002240.3:p.Asp348Tyr
NM_170782.3:c.127G>T	NP_740752.1:p.Asp43Tyr
NM_001204087.2:c.1042G>T	NP_001191016.1:p.Asp348Tyr