Canonical Allele Identifier: CA1883843301

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135750132T= , CM000671.2:g.135750132T=	GRCh38
NC_000009.11:g.138641978T= , CM000671.1:g.138641978T=	GRCh37
NC_000009.10:g.137781799T=	NCBI36
NG_033070.1:g.52948T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.289T= MANE Select	ENSP00000360822.2:p.Phe97=
ENST00000637018.1:n.94T=
ENST00000638123.1:n.24T=
ENST00000674572.1:c.130T=	ENSP00000501742.1:p.Phe44=
ENST00000675090.1:c.37T=	ENSP00000501833.1:p.Phe13=
ENST00000675399.1:c.37T=	ENSP00000501932.1:p.Phe13=
ENST00000676421.1:c.37T=	ENSP00000502322.1:p.Phe13=
ENST00000263604.5:c.190T=	ENSP00000263604.4:p.Phe64=
ENST00000371757.6:c.289T=	ENSP00000360822.2:p.Phe97=
ENST00000460750.5:c.289T=	ENSP00000418777.1:p.Phe97=
ENST00000473941.5:c.130T=	ENSP00000420764.1:p.Phe44=
ENST00000486577.6:c.172T=	ENSP00000417578.3:p.Phe58=
ENST00000487664.5:c.289T=	ENSP00000417851.2:p.Phe97=
ENST00000488444.6:c.232T=	ENSP00000419007.3:p.Phe78=
ENST00000490355.6:c.232T=	ENSP00000418003.3:p.Phe78=
ENST00000491806.6:c.232T=	ENSP00000419086.3:p.Phe78=
ENST00000628528.2:c.145T=	ENSP00000486374.1:p.Phe49=
ENST00000630792.2:c.130T=	ENSP00000486486.1:p.Phe44=
ENST00000631073.2:c.232T=	ENSP00000486130.1:p.Phe78=
NM_001272003.1:c.145T=	NP_001258932.1:p.Phe49=
NM_020822.2:c.289T=	NP_065873.2:p.Phe97=
XM_011518877.1:c.424T=	XP_011517179.1:p.Phe142=
XM_011518878.1:c.424T=	XP_011517180.1:p.Phe142=
XM_011518879.1:c.424T=	XP_011517181.1:p.Phe142=
XM_011518880.1:c.190T=	XP_011517182.1:p.Phe64=
XM_011518877.3:c.424T=	XP_011517179.1:p.Phe142=
XM_011518878.3:c.424T=	XP_011517180.1:p.Phe142=
XM_011518879.3:c.424T=	XP_011517181.1:p.Phe142=
XM_017014931.1:c.314T=	XP_016870420.1:p.Leu105=
XM_017014932.1:c.37T=	XP_016870421.1:p.Phe13=
XM_017014933.1:c.-131T=	XP_016870422.1:n.-131T=
XM_024447617.1:c.-231T=	XP_024303385.1:n.-231T=
XM_024447618.1:c.-231T=	XP_024303386.1:n.-231T=
NM_020822.3:c.289T= MANE Select	NP_065873.2:p.Phe97=
NM_001272003.2:c.145T=	NP_001258932.1:p.Phe49=