Canonical Allele Identifier: CA1883863418

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135759686G= , CM000671.2:g.135759686G=	GRCh38
NC_000009.11:g.138651532G= , CM000671.1:g.138651532G=	GRCh37
NC_000009.10:g.137791353G=	NCBI36
NG_033070.1:g.62502G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.862G= MANE Select	ENSP00000360822.2:p.Gly288=
ENST00000674572.1:c.703G=	ENSP00000501742.1:p.Gly235=
ENST00000675090.1:c.610G=	ENSP00000501833.1:p.Gly204=
ENST00000675399.1:c.610G=	ENSP00000501932.1:p.Gly204=
ENST00000676421.1:c.619G=	ENSP00000502322.1:p.Gly207=
ENST00000263604.5:c.763G=	ENSP00000263604.4:p.Gly255=
ENST00000371757.6:c.862G=	ENSP00000360822.2:p.Gly288=
ENST00000460750.5:c.*472G=	ENSP00000418777.1:n.*472G=
ENST00000473941.5:c.703G=	ENSP00000420764.1:p.Gly235=
ENST00000486577.6:c.745G=	ENSP00000417578.3:p.Gly249=
ENST00000487664.5:c.862G=	ENSP00000417851.2:p.Gly288=
ENST00000488444.6:c.805G=	ENSP00000419007.3:p.Gly269=
ENST00000490355.6:c.805G=	ENSP00000418003.3:p.Gly269=
ENST00000490363.3:n.681G=
ENST00000491806.6:c.805G=	ENSP00000419086.3:p.Gly269=
ENST00000628528.2:c.727G=	ENSP00000486374.1:p.Gly243=
ENST00000630792.2:c.703G=	ENSP00000486486.1:p.Gly235=
ENST00000631073.2:c.805G=	ENSP00000486130.1:p.Gly269=
NM_001272003.1:c.727G=	NP_001258932.1:p.Gly243=
NM_020822.2:c.862G=	NP_065873.2:p.Gly288=
XM_011518877.1:c.997G=	XP_011517179.1:p.Gly333=
XM_011518878.1:c.1006G=	XP_011517180.1:p.Gly336=
XM_011518879.1:c.997G=	XP_011517181.1:p.Gly333=
XM_011518880.1:c.763G=	XP_011517182.1:p.Gly255=
XM_011518881.1:c.352G=	XP_011517183.1:p.Gly118=
XM_011518877.3:c.997G=	XP_011517179.1:p.Gly333=
XM_011518878.3:c.1006G=	XP_011517180.1:p.Gly336=
XM_011518879.3:c.997G=	XP_011517181.1:p.Gly333=
XM_011518881.3:c.352G=	XP_011517183.1:p.Gly118=
XM_017014931.1:c.796G=	XP_016870420.1:p.Gly266=
XM_017014932.1:c.619G=	XP_016870421.1:p.Gly207=
XM_017014933.1:c.352G=	XP_016870422.1:p.Gly118=
XM_024447617.1:c.352G=	XP_024303385.1:p.Gly118=
XM_024447618.1:c.352G=	XP_024303386.1:p.Gly118=
NM_020822.3:c.862G= MANE Select	NP_065873.2:p.Gly288=
NM_001272003.2:c.727G=	NP_001258932.1:p.Gly243=