Canonical Allele Identifier: CA1883884683

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775310G= , CM000671.2:g.135775310G=	GRCh38
NC_000009.11:g.138667156G= , CM000671.1:g.138667156G=	GRCh37
NC_000009.10:g.137806977G=	NCBI36
NG_033070.1:g.78126G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2244G= MANE Select	ENSP00000360822.2:p.Glu748=
ENST00000674572.1:c.2085G=	ENSP00000501742.1:p.Glu695=
ENST00000675090.1:c.1992G=	ENSP00000501833.1:p.Glu664=
ENST00000675399.1:c.1992G=	ENSP00000501932.1:p.Glu664=
ENST00000676421.1:c.2001G=	ENSP00000502322.1:p.Glu667=
ENST00000263604.5:c.2145G=	ENSP00000263604.4:p.Glu715=
ENST00000371757.6:c.2244G=	ENSP00000360822.2:p.Glu748=
ENST00000460750.5:c.*1854G=	ENSP00000418777.1:n.*1854G=
ENST00000486577.6:c.2127G=	ENSP00000417578.3:p.Glu709=
ENST00000487664.5:c.2244G=	ENSP00000417851.2:p.Glu748=
ENST00000488444.6:c.2187G=	ENSP00000419007.3:p.Glu729=
ENST00000490355.6:c.2181G=	ENSP00000418003.3:p.Glu727=
ENST00000490363.3:n.2063G=
ENST00000491806.6:c.2187G=	ENSP00000419086.3:p.Glu729=
ENST00000628528.2:c.2109G=	ENSP00000486374.1:p.Glu703=
ENST00000630792.2:c.2079G=	ENSP00000486486.1:p.Glu693=
ENST00000631073.2:c.2187G=	ENSP00000486130.1:p.Glu729=
ENST00000631193.1:c.93G=	ENSP00000486830.1:p.Glu31=
NM_001272003.1:c.2109G=	NP_001258932.1:p.Glu703=
NM_020822.2:c.2244G=	NP_065873.2:p.Glu748=
XM_011518877.1:c.2379G=	XP_011517179.1:p.Glu793=
XM_011518878.1:c.2388G=	XP_011517180.1:p.Glu796=
XM_011518879.1:c.2379G=	XP_011517181.1:p.Glu793=
XM_011518880.1:c.2145G=	XP_011517182.1:p.Glu715=
XM_011518881.1:c.1734G=	XP_011517183.1:p.Glu578=
XM_011518877.3:c.2379G=	XP_011517179.1:p.Glu793=
XM_011518878.3:c.2388G=	XP_011517180.1:p.Glu796=
XM_011518879.3:c.2379G=	XP_011517181.1:p.Glu793=
XM_011518881.3:c.1734G=	XP_011517183.1:p.Glu578=
XM_017014931.1:c.2178G=	XP_016870420.1:p.Glu726=
XM_017014932.1:c.2001G=	XP_016870421.1:p.Glu667=
XM_017014933.1:c.1734G=	XP_016870422.1:p.Glu578=
XM_024447617.1:c.1734G=	XP_024303385.1:p.Glu578=
XM_024447618.1:c.1734G=	XP_024303386.1:p.Glu578=
NM_020822.3:c.2244G= MANE Select	NP_065873.2:p.Glu748=
NM_001272003.2:c.2109G=	NP_001258932.1:p.Glu703=