Canonical Allele Identifier: CA344080859

Gene: KCNT2

Linked Data

• MyVariant Identifiers: chr1:g.196398715G>T (hg19) ; chr1:g.196429585G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196429585G>T , CM000663.2:g.196429585G>T	GRCh38
NC_000001.10:g.196398715G>T , CM000663.1:g.196398715G>T	GRCh37
NC_000001.9:g.194665338G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000294725.14:c.811C>A MANE Select	ENSP00000294725.8:p.Pro271Thr
ENST00000647658.1:c.811C>A	ENSP00000496885.1:p.Pro271Thr
ENST00000294725.13:c.811C>A	ENSP00000294725.8:p.Pro271Thr
ENST00000367433.9:c.811C>A	ENSP00000356403.5:p.Pro271Thr
ENST00000451324.6:c.19-30914C>A	ENSP00000405474.2:n.19-30914C>A
ENST00000498426.5:n.268C>A
ENST00000609185.5:c.811C>A	ENSP00000476657.1:p.Pro271Thr
ENST00000610076.1:n.987C>A
NM_001287819.1:c.811C>A	NP_001274748.1:p.Pro271Thr
NM_001287820.1:c.811C>A	NP_001274749.1:p.Pro271Thr
NM_198503.3:c.811C>A	NP_940905.2:p.Pro271Thr
XM_006711294.1:c.811C>A	XP_006711357.1:p.Pro271Thr
XM_006711295.1:c.811C>A	XP_006711358.1:p.Pro271Thr
XM_011509482.1:c.736C>A	XP_011507784.1:p.Pro246Thr
XM_011509483.1:c.811C>A	XP_011507785.1:p.Pro271Thr
XR_921773.1:n.1062C>A
XR_921774.1:n.1062C>A
XR_921775.1:n.1062C>A
NM_001287819.2:c.811C>A	NP_001274748.1:p.Pro271Thr
NM_001287820.2:c.811C>A	NP_001274749.1:p.Pro271Thr
NM_198503.4:c.811C>A	NP_940905.2:p.Pro271Thr
NR_146057.1:n.1078C>A
NR_146058.1:n.1078C>A
XM_006711294.3:c.811C>A	XP_006711357.1:p.Pro271Thr
XM_006711295.3:c.811C>A	XP_006711358.1:p.Pro271Thr
XM_011509483.3:c.811C>A	XP_011507785.1:p.Pro271Thr
XM_017001179.2:c.811C>A	XP_016856668.1:p.Pro271Thr
XM_017001180.2:c.811C>A	XP_016856669.1:p.Pro271Thr
XM_017001185.2:c.736C>A	XP_016856674.1:p.Pro246Thr
XM_024446697.1:c.-518C>A	XP_024302465.1:n.-518C>A
XR_001737149.2:n.1062C>A
XR_001737151.2:n.1062C>A
XR_921774.3:n.1062C>A
NM_001287819.3:c.811C>A	NP_001274748.1:p.Pro271Thr
NM_001287820.3:c.811C>A	NP_001274749.1:p.Pro271Thr
NM_198503.5:c.811C>A MANE Select	NP_940905.2:p.Pro271Thr
NR_146057.2:n.942C>A
NR_146058.2:n.942C>A