Canonical Allele Identifier: CA1883884964

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775395_135775405delinsTGCTGCCTGCG , CM000671.2:g.135775395_135775405delinsTGCTGCCTGCG	GRCh38
NC_000009.11:g.138667241_138667251delinsTGCTGCCTGCG , CM000671.1:g.138667241_138667251delinsTGCTGCCTGCG	GRCh37
NC_000009.10:g.137807062_137807072delinsTGCTGCCTGCG	NCBI36
NG_033070.1:g.78211_78221delinsTGCTGCCTGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2329_2339delinsTGCTGCCTGCG MANE Select	ENSP00000360822.2:p.Cys777=
ENST00000674572.1:c.2170_2180delinsTGCTGCCTGCG	ENSP00000501742.1:p.Cys724=
ENST00000675090.1:c.2077_2087delinsTGCTGCCTGCG	ENSP00000501833.1:p.Cys693=
ENST00000675399.1:c.2077_2087delinsTGCTGCCTGCG	ENSP00000501932.1:p.Cys693=
ENST00000676421.1:c.2086_2096delinsTGCTGCCTGCG	ENSP00000502322.1:p.Cys696=
ENST00000263604.5:c.2230_2240delinsTGCTGCCTGCG	ENSP00000263604.4:p.Cys744=
ENST00000371757.6:c.2329_2339delinsTGCTGCCTGCG	ENSP00000360822.2:p.Cys777=
ENST00000460750.5:c.*1939_*1949delinsTGCTGCCTGCG	ENSP00000418777.1:n.*1939_*1949delinsTGCTGCCTGCG
ENST00000486577.6:c.2212_2222delinsTGCTGCCTGCG	ENSP00000417578.3:p.Cys738=
ENST00000487664.5:c.2329_2339delinsTGCTGCCTGCG	ENSP00000417851.2:p.Cys777=
ENST00000488444.6:c.2272_2282delinsTGCTGCCTGCG	ENSP00000419007.3:p.Cys758=
ENST00000490355.6:c.2266_2276delinsTGCTGCCTGCG	ENSP00000418003.3:p.Cys756=
ENST00000490363.3:n.2148_2158delinsTGCTGCCTGCG
ENST00000491806.6:c.2272_2282delinsTGCTGCCTGCG	ENSP00000419086.3:p.Cys758=
ENST00000628528.2:c.2194_2204delinsTGCTGCCTGCG	ENSP00000486374.1:p.Cys732=
ENST00000630792.2:c.2164_2174delinsTGCTGCCTGCG	ENSP00000486486.1:p.Cys722=
ENST00000631073.2:c.2272_2282delinsTGCTGCCTGCG	ENSP00000486130.1:p.Cys758=
ENST00000631193.1:c.178_188delinsTGCTGCCTGCG	ENSP00000486830.1:p.Cys60=
NM_001272003.1:c.2194_2204delinsTGCTGCCTGCG	NP_001258932.1:p.Cys732=
NM_020822.2:c.2329_2339delinsTGCTGCCTGCG	NP_065873.2:p.Cys777=
XM_011518877.1:c.2464_2474delinsTGCTGCCTGCG	XP_011517179.1:p.Cys822=
XM_011518878.1:c.2473_2483delinsTGCTGCCTGCG	XP_011517180.1:p.Cys825=
XM_011518879.1:c.2464_2474delinsTGCTGCCTGCG	XP_011517181.1:p.Cys822=
XM_011518880.1:c.2230_2240delinsTGCTGCCTGCG	XP_011517182.1:p.Cys744=
XM_011518881.1:c.1819_1829delinsTGCTGCCTGCG	XP_011517183.1:p.Cys607=
XM_011518877.3:c.2464_2474delinsTGCTGCCTGCG	XP_011517179.1:p.Cys822=
XM_011518878.3:c.2473_2483delinsTGCTGCCTGCG	XP_011517180.1:p.Cys825=
XM_011518879.3:c.2464_2474delinsTGCTGCCTGCG	XP_011517181.1:p.Cys822=
XM_011518881.3:c.1819_1829delinsTGCTGCCTGCG	XP_011517183.1:p.Cys607=
XM_017014931.1:c.2263_2273delinsTGCTGCCTGCG	XP_016870420.1:p.Cys755=
XM_017014932.1:c.2086_2096delinsTGCTGCCTGCG	XP_016870421.1:p.Cys696=
XM_017014933.1:c.1819_1829delinsTGCTGCCTGCG	XP_016870422.1:p.Cys607=
XM_024447617.1:c.1819_1829delinsTGCTGCCTGCG	XP_024303385.1:p.Cys607=
XM_024447618.1:c.1819_1829delinsTGCTGCCTGCG	XP_024303386.1:p.Cys607=
NM_020822.3:c.2329_2339delinsTGCTGCCTGCG MANE Select	NP_065873.2:p.Cys777=
NM_001272003.2:c.2194_2204delinsTGCTGCCTGCG	NP_001258932.1:p.Cys732=