Canonical Allele Identifier: CA344080845

Gene: KCNT2

Linked Data

• MyVariant Identifiers: chr1:g.196398709G>A (hg19) ; chr1:g.196429579G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196429579G>A , CM000663.2:g.196429579G>A	GRCh38
NC_000001.10:g.196398709G>A , CM000663.1:g.196398709G>A	GRCh37
NC_000001.9:g.194665332G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000294725.14:c.817C>T MANE Select	ENSP00000294725.8:p.Gln273Ter
ENST00000647658.1:c.817C>T	ENSP00000496885.1:p.Gln273Ter
ENST00000294725.13:c.817C>T	ENSP00000294725.8:p.Gln273Ter
ENST00000367433.9:c.817C>T	ENSP00000356403.5:p.Gln273Ter
ENST00000451324.6:c.19-30908C>T	ENSP00000405474.2:n.19-30908C>T
ENST00000498426.5:n.274C>T
ENST00000609185.5:c.817C>T	ENSP00000476657.1:p.Gln273Ter
ENST00000610076.1:n.993C>T
NM_001287819.1:c.817C>T	NP_001274748.1:p.Gln273Ter
NM_001287820.1:c.817C>T	NP_001274749.1:p.Gln273Ter
NM_198503.3:c.817C>T	NP_940905.2:p.Gln273Ter
XM_006711294.1:c.817C>T	XP_006711357.1:p.Gln273Ter
XM_006711295.1:c.817C>T	XP_006711358.1:p.Gln273Ter
XM_011509482.1:c.742C>T	XP_011507784.1:p.Gln248Ter
XM_011509483.1:c.817C>T	XP_011507785.1:p.Gln273Ter
XR_921773.1:n.1068C>T
XR_921774.1:n.1068C>T
XR_921775.1:n.1068C>T
NM_001287819.2:c.817C>T	NP_001274748.1:p.Gln273Ter
NM_001287820.2:c.817C>T	NP_001274749.1:p.Gln273Ter
NM_198503.4:c.817C>T	NP_940905.2:p.Gln273Ter
NR_146057.1:n.1084C>T
NR_146058.1:n.1084C>T
XM_006711294.3:c.817C>T	XP_006711357.1:p.Gln273Ter
XM_006711295.3:c.817C>T	XP_006711358.1:p.Gln273Ter
XM_011509483.3:c.817C>T	XP_011507785.1:p.Gln273Ter
XM_017001179.2:c.817C>T	XP_016856668.1:p.Gln273Ter
XM_017001180.2:c.817C>T	XP_016856669.1:p.Gln273Ter
XM_017001185.2:c.742C>T	XP_016856674.1:p.Gln248Ter
XM_024446697.1:c.-512C>T	XP_024302465.1:n.-512C>T
XR_001737149.2:n.1068C>T
XR_001737151.2:n.1068C>T
XR_921774.3:n.1068C>T
NM_001287819.3:c.817C>T	NP_001274748.1:p.Gln273Ter
NM_001287820.3:c.817C>T	NP_001274749.1:p.Gln273Ter
NM_198503.5:c.817C>T MANE Select	NP_940905.2:p.Gln273Ter
NR_146057.2:n.948C>T
NR_146058.2:n.948C>T