Canonical Allele Identifier: CA1883884697

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775322C= , CM000671.2:g.135775322C=	GRCh38
NC_000009.11:g.138667168C= , CM000671.1:g.138667168C=	GRCh37
NC_000009.10:g.137806989C=	NCBI36
NG_033070.1:g.78138C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2256C= MANE Select	ENSP00000360822.2:p.Gly752=
ENST00000674572.1:c.2097C=	ENSP00000501742.1:p.Gly699=
ENST00000675090.1:c.2004C=	ENSP00000501833.1:p.Gly668=
ENST00000675399.1:c.2004C=	ENSP00000501932.1:p.Gly668=
ENST00000676421.1:c.2013C=	ENSP00000502322.1:p.Gly671=
ENST00000263604.5:c.2157C=	ENSP00000263604.4:p.Gly719=
ENST00000371757.6:c.2256C=	ENSP00000360822.2:p.Gly752=
ENST00000460750.5:c.*1866C=	ENSP00000418777.1:n.*1866C=
ENST00000486577.6:c.2139C=	ENSP00000417578.3:p.Gly713=
ENST00000487664.5:c.2256C=	ENSP00000417851.2:p.Gly752=
ENST00000488444.6:c.2199C=	ENSP00000419007.3:p.Gly733=
ENST00000490355.6:c.2193C=	ENSP00000418003.3:p.Gly731=
ENST00000490363.3:n.2075C=
ENST00000491806.6:c.2199C=	ENSP00000419086.3:p.Gly733=
ENST00000628528.2:c.2121C=	ENSP00000486374.1:p.Gly707=
ENST00000630792.2:c.2091C=	ENSP00000486486.1:p.Gly697=
ENST00000631073.2:c.2199C=	ENSP00000486130.1:p.Gly733=
ENST00000631193.1:c.105C=	ENSP00000486830.1:p.Gly35=
NM_001272003.1:c.2121C=	NP_001258932.1:p.Gly707=
NM_020822.2:c.2256C=	NP_065873.2:p.Gly752=
XM_011518877.1:c.2391C=	XP_011517179.1:p.Gly797=
XM_011518878.1:c.2400C=	XP_011517180.1:p.Gly800=
XM_011518879.1:c.2391C=	XP_011517181.1:p.Gly797=
XM_011518880.1:c.2157C=	XP_011517182.1:p.Gly719=
XM_011518881.1:c.1746C=	XP_011517183.1:p.Gly582=
XM_011518877.3:c.2391C=	XP_011517179.1:p.Gly797=
XM_011518878.3:c.2400C=	XP_011517180.1:p.Gly800=
XM_011518879.3:c.2391C=	XP_011517181.1:p.Gly797=
XM_011518881.3:c.1746C=	XP_011517183.1:p.Gly582=
XM_017014931.1:c.2190C=	XP_016870420.1:p.Gly730=
XM_017014932.1:c.2013C=	XP_016870421.1:p.Gly671=
XM_017014933.1:c.1746C=	XP_016870422.1:p.Gly582=
XM_024447617.1:c.1746C=	XP_024303385.1:p.Gly582=
XM_024447618.1:c.1746C=	XP_024303386.1:p.Gly582=
NM_020822.3:c.2256C= MANE Select	NP_065873.2:p.Gly752=
NM_001272003.2:c.2121C=	NP_001258932.1:p.Gly707=