Canonical Allele Identifier: CA1883866221

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135764920G= , CM000671.2:g.135764920G=	GRCh38
NC_000009.11:g.138656766G= , CM000671.1:g.138656766G=	GRCh37
NC_000009.10:g.137796587G=	NCBI36
NG_033070.1:g.67736G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371757.7:c.1036-111G= MANE Select	ENSP00000360822.2:n.1036-111G=
ENST00000674572.1:c.877-111G=	ENSP00000501742.1:n.877-111G=
ENST00000675090.1:c.784-111G=	ENSP00000501833.1:n.784-111G=
ENST00000675399.1:c.784-111G=	ENSP00000501932.1:n.784-111G=
ENST00000676421.1:c.793-111G=	ENSP00000502322.1:n.793-111G=
ENST00000263604.5:c.937-111G=	ENSP00000263604.4:n.937-111G=
ENST00000371757.6:c.1036-111G=	ENSP00000360822.2:n.1036-111G=
ENST00000460750.5:c.*646-111G=	ENSP00000418777.1:n.*646-111G=
ENST00000486577.6:c.919-111G=	ENSP00000417578.3:n.919-111G=
ENST00000487664.5:c.1036-111G=	ENSP00000417851.2:n.1036-111G=
ENST00000488444.6:c.979-111G=	ENSP00000419007.3:n.979-111G=
ENST00000490355.6:c.979-111G=	ENSP00000418003.3:n.979-111G=
ENST00000490363.3:n.855-111G=
ENST00000491806.6:c.979-111G=	ENSP00000419086.3:n.979-111G=
ENST00000628528.2:c.901-111G=	ENSP00000486374.1:n.901-111G=
ENST00000630792.2:c.877-111G=	ENSP00000486486.1:n.877-111G=
ENST00000631073.2:c.979-111G=	ENSP00000486130.1:n.979-111G=
NM_001272003.1:c.901-111G=	NP_001258932.1:n.901-111G=
NM_020822.2:c.1036-111G=	NP_065873.2:n.1036-111G=
XM_011518877.1:c.1171-111G=	XP_011517179.1:n.1171-111G=
XM_011518878.1:c.1180-111G=	XP_011517180.1:n.1180-111G=
XM_011518879.1:c.1171-111G=	XP_011517181.1:n.1171-111G=
XM_011518880.1:c.937-111G=	XP_011517182.1:n.937-111G=
XM_011518881.1:c.526-111G=	XP_011517183.1:n.526-111G=
XM_011518877.3:c.1171-111G=	XP_011517179.1:n.1171-111G=
XM_011518878.3:c.1180-111G=	XP_011517180.1:n.1180-111G=
XM_011518879.3:c.1171-111G=	XP_011517181.1:n.1171-111G=
XM_011518881.3:c.526-111G=	XP_011517183.1:n.526-111G=
XM_017014931.1:c.970-111G=	XP_016870420.1:n.970-111G=
XM_017014932.1:c.793-111G=	XP_016870421.1:n.793-111G=
XM_017014933.1:c.526-111G=	XP_016870422.1:n.526-111G=
XM_024447617.1:c.526-111G=	XP_024303385.1:n.526-111G=
XM_024447618.1:c.526-111G=	XP_024303386.1:n.526-111G=
NM_020822.3:c.1036-111G= MANE Select	NP_065873.2:n.1036-111G=
NM_001272003.2:c.901-111G=	NP_001258932.1:n.901-111G=