Canonical Allele Identifier: CA1883872504

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770003T= , CM000671.2:g.135770003T=	GRCh38
NC_000009.11:g.138661849T= , CM000671.1:g.138661849T=	GRCh37
NC_000009.10:g.137801670T=	NCBI36
NG_033070.1:g.72819T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1567T= MANE Select	ENSP00000360822.2:p.Cys523=
ENST00000674572.1:c.1408T=	ENSP00000501742.1:p.Cys470=
ENST00000675090.1:c.1315T=	ENSP00000501833.1:p.Cys439=
ENST00000675399.1:c.1315T=	ENSP00000501932.1:p.Cys439=
ENST00000676421.1:c.1324T=	ENSP00000502322.1:p.Cys442=
ENST00000263604.5:c.1468T=	ENSP00000263604.4:p.Cys490=
ENST00000371757.6:c.1567T=	ENSP00000360822.2:p.Cys523=
ENST00000460750.5:c.*1177T=	ENSP00000418777.1:n.*1177T=
ENST00000486577.6:c.1450T=	ENSP00000417578.3:p.Cys484=
ENST00000487664.5:c.1567T=	ENSP00000417851.2:p.Cys523=
ENST00000488444.6:c.1510T=	ENSP00000419007.3:p.Cys504=
ENST00000490355.6:c.1510T=	ENSP00000418003.3:p.Cys504=
ENST00000490363.3:n.1386T=
ENST00000491806.6:c.1510T=	ENSP00000419086.3:p.Cys504=
ENST00000628528.2:c.1432T=	ENSP00000486374.1:p.Cys478=
ENST00000630792.2:c.1408T=	ENSP00000486486.1:p.Cys470=
ENST00000631073.2:c.1510T=	ENSP00000486130.1:p.Cys504=
NM_001272003.1:c.1432T=	NP_001258932.1:p.Cys478=
NM_020822.2:c.1567T=	NP_065873.2:p.Cys523=
XM_011518877.1:c.1702T=	XP_011517179.1:p.Cys568=
XM_011518878.1:c.1711T=	XP_011517180.1:p.Cys571=
XM_011518879.1:c.1702T=	XP_011517181.1:p.Cys568=
XM_011518880.1:c.1468T=	XP_011517182.1:p.Cys490=
XM_011518881.1:c.1057T=	XP_011517183.1:p.Cys353=
XM_011518877.3:c.1702T=	XP_011517179.1:p.Cys568=
XM_011518878.3:c.1711T=	XP_011517180.1:p.Cys571=
XM_011518879.3:c.1702T=	XP_011517181.1:p.Cys568=
XM_011518881.3:c.1057T=	XP_011517183.1:p.Cys353=
XM_017014931.1:c.1501T=	XP_016870420.1:p.Cys501=
XM_017014932.1:c.1324T=	XP_016870421.1:p.Cys442=
XM_017014933.1:c.1057T=	XP_016870422.1:p.Cys353=
XM_024447617.1:c.1057T=	XP_024303385.1:p.Cys353=
XM_024447618.1:c.1057T=	XP_024303386.1:p.Cys353=
NM_020822.3:c.1567T= MANE Select	NP_065873.2:p.Cys523=
NM_001272003.2:c.1432T=	NP_001258932.1:p.Cys478=