Canonical Allele Identifier: CA1883884840

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775359A= , CM000671.2:g.135775359A=	GRCh38
NC_000009.11:g.138667205A= , CM000671.1:g.138667205A=	GRCh37
NC_000009.10:g.137807026A=	NCBI36
NG_033070.1:g.78175A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2293A= MANE Select	ENSP00000360822.2:p.Thr765=
ENST00000674572.1:c.2134A=	ENSP00000501742.1:p.Thr712=
ENST00000675090.1:c.2041A=	ENSP00000501833.1:p.Thr681=
ENST00000675399.1:c.2041A=	ENSP00000501932.1:p.Thr681=
ENST00000676421.1:c.2050A=	ENSP00000502322.1:p.Thr684=
ENST00000263604.5:c.2194A=	ENSP00000263604.4:p.Thr732=
ENST00000371757.6:c.2293A=	ENSP00000360822.2:p.Thr765=
ENST00000460750.5:c.*1903A=	ENSP00000418777.1:n.*1903A=
ENST00000486577.6:c.2176A=	ENSP00000417578.3:p.Thr726=
ENST00000487664.5:c.2293A=	ENSP00000417851.2:p.Thr765=
ENST00000488444.6:c.2236A=	ENSP00000419007.3:p.Thr746=
ENST00000490355.6:c.2230A=	ENSP00000418003.3:p.Thr744=
ENST00000490363.3:n.2112A=
ENST00000491806.6:c.2236A=	ENSP00000419086.3:p.Thr746=
ENST00000628528.2:c.2158A=	ENSP00000486374.1:p.Thr720=
ENST00000630792.2:c.2128A=	ENSP00000486486.1:p.Thr710=
ENST00000631073.2:c.2236A=	ENSP00000486130.1:p.Thr746=
ENST00000631193.1:c.142A=	ENSP00000486830.1:p.Thr48=
NM_001272003.1:c.2158A=	NP_001258932.1:p.Thr720=
NM_020822.2:c.2293A=	NP_065873.2:p.Thr765=
XM_011518877.1:c.2428A=	XP_011517179.1:p.Thr810=
XM_011518878.1:c.2437A=	XP_011517180.1:p.Thr813=
XM_011518879.1:c.2428A=	XP_011517181.1:p.Thr810=
XM_011518880.1:c.2194A=	XP_011517182.1:p.Thr732=
XM_011518881.1:c.1783A=	XP_011517183.1:p.Thr595=
XM_011518877.3:c.2428A=	XP_011517179.1:p.Thr810=
XM_011518878.3:c.2437A=	XP_011517180.1:p.Thr813=
XM_011518879.3:c.2428A=	XP_011517181.1:p.Thr810=
XM_011518881.3:c.1783A=	XP_011517183.1:p.Thr595=
XM_017014931.1:c.2227A=	XP_016870420.1:p.Thr743=
XM_017014932.1:c.2050A=	XP_016870421.1:p.Thr684=
XM_017014933.1:c.1783A=	XP_016870422.1:p.Thr595=
XM_024447617.1:c.1783A=	XP_024303385.1:p.Thr595=
XM_024447618.1:c.1783A=	XP_024303386.1:p.Thr595=
NM_020822.3:c.2293A= MANE Select	NP_065873.2:p.Thr765=
NM_001272003.2:c.2158A=	NP_001258932.1:p.Thr720=