Canonical Allele Identifier: CA1883884849
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135775361C= , CM000671.2:g.135775361C= GRCh38
NC_000009.11:g.138667207C= , CM000671.1:g.138667207C= GRCh37
NC_000009.10:g.137807028C= NCBI36
NG_033070.1:g.78177C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.2295C= MANE Select ENSP00000360822.2:p.Thr765=
ENST00000674572.1:c.2136C= ENSP00000501742.1:p.Thr712=
ENST00000675090.1:c.2043C= ENSP00000501833.1:p.Thr681=
ENST00000675399.1:c.2043C= ENSP00000501932.1:p.Thr681=
ENST00000676421.1:c.2052C= ENSP00000502322.1:p.Thr684=
ENST00000263604.5:c.2196C= ENSP00000263604.4:p.Thr732=
ENST00000371757.6:c.2295C= ENSP00000360822.2:p.Thr765=
ENST00000460750.5:c.*1905C= ENSP00000418777.1:n.*1905C=
ENST00000486577.6:c.2178C= ENSP00000417578.3:p.Thr726=
ENST00000487664.5:c.2295C= ENSP00000417851.2:p.Thr765=
ENST00000488444.6:c.2238C= ENSP00000419007.3:p.Thr746=
ENST00000490355.6:c.2232C= ENSP00000418003.3:p.Thr744=
ENST00000490363.3:n.2114C=
ENST00000491806.6:c.2238C= ENSP00000419086.3:p.Thr746=
ENST00000628528.2:c.2160C= ENSP00000486374.1:p.Thr720=
ENST00000630792.2:c.2130C= ENSP00000486486.1:p.Thr710=
ENST00000631073.2:c.2238C= ENSP00000486130.1:p.Thr746=
ENST00000631193.1:c.144C= ENSP00000486830.1:p.Thr48=
NM_001272003.1:c.2160C= NP_001258932.1:p.Thr720=
NM_020822.2:c.2295C= NP_065873.2:p.Thr765=
XM_011518877.1:c.2430C= XP_011517179.1:p.Thr810=
XM_011518878.1:c.2439C= XP_011517180.1:p.Thr813=
XM_011518879.1:c.2430C= XP_011517181.1:p.Thr810=
XM_011518880.1:c.2196C= XP_011517182.1:p.Thr732=
XM_011518881.1:c.1785C= XP_011517183.1:p.Thr595=
XM_011518877.3:c.2430C= XP_011517179.1:p.Thr810=
XM_011518878.3:c.2439C= XP_011517180.1:p.Thr813=
XM_011518879.3:c.2430C= XP_011517181.1:p.Thr810=
XM_011518881.3:c.1785C= XP_011517183.1:p.Thr595=
XM_017014931.1:c.2229C= XP_016870420.1:p.Thr743=
XM_017014932.1:c.2052C= XP_016870421.1:p.Thr684=
XM_017014933.1:c.1785C= XP_016870422.1:p.Thr595=
XM_024447617.1:c.1785C= XP_024303385.1:p.Thr595=
XM_024447618.1:c.1785C= XP_024303386.1:p.Thr595=
NM_020822.3:c.2295C= MANE Select NP_065873.2:p.Thr765=
NM_001272003.2:c.2160C= NP_001258932.1:p.Thr720=