Canonical Allele Identifier: CA1883884897
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135775374C= , CM000671.2:g.135775374C= GRCh38
NC_000009.11:g.138667220C= , CM000671.1:g.138667220C= GRCh37
NC_000009.10:g.137807041C= NCBI36
NG_033070.1:g.78190C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.2308C= MANE Select ENSP00000360822.2:p.Leu770=
ENST00000674572.1:c.2149C= ENSP00000501742.1:p.Leu717=
ENST00000675090.1:c.2056C= ENSP00000501833.1:p.Leu686=
ENST00000675399.1:c.2056C= ENSP00000501932.1:p.Leu686=
ENST00000676421.1:c.2065C= ENSP00000502322.1:p.Leu689=
ENST00000263604.5:c.2209C= ENSP00000263604.4:p.Leu737=
ENST00000371757.6:c.2308C= ENSP00000360822.2:p.Leu770=
ENST00000460750.5:c.*1918C= ENSP00000418777.1:n.*1918C=
ENST00000486577.6:c.2191C= ENSP00000417578.3:p.Leu731=
ENST00000487664.5:c.2308C= ENSP00000417851.2:p.Leu770=
ENST00000488444.6:c.2251C= ENSP00000419007.3:p.Leu751=
ENST00000490355.6:c.2245C= ENSP00000418003.3:p.Leu749=
ENST00000490363.3:n.2127C=
ENST00000491806.6:c.2251C= ENSP00000419086.3:p.Leu751=
ENST00000628528.2:c.2173C= ENSP00000486374.1:p.Leu725=
ENST00000630792.2:c.2143C= ENSP00000486486.1:p.Leu715=
ENST00000631073.2:c.2251C= ENSP00000486130.1:p.Leu751=
ENST00000631193.1:c.157C= ENSP00000486830.1:p.Leu53=
NM_001272003.1:c.2173C= NP_001258932.1:p.Leu725=
NM_020822.2:c.2308C= NP_065873.2:p.Leu770=
XM_011518877.1:c.2443C= XP_011517179.1:p.Leu815=
XM_011518878.1:c.2452C= XP_011517180.1:p.Leu818=
XM_011518879.1:c.2443C= XP_011517181.1:p.Leu815=
XM_011518880.1:c.2209C= XP_011517182.1:p.Leu737=
XM_011518881.1:c.1798C= XP_011517183.1:p.Leu600=
XM_011518877.3:c.2443C= XP_011517179.1:p.Leu815=
XM_011518878.3:c.2452C= XP_011517180.1:p.Leu818=
XM_011518879.3:c.2443C= XP_011517181.1:p.Leu815=
XM_011518881.3:c.1798C= XP_011517183.1:p.Leu600=
XM_017014931.1:c.2242C= XP_016870420.1:p.Leu748=
XM_017014932.1:c.2065C= XP_016870421.1:p.Leu689=
XM_017014933.1:c.1798C= XP_016870422.1:p.Leu600=
XM_024447617.1:c.1798C= XP_024303385.1:p.Leu600=
XM_024447618.1:c.1798C= XP_024303386.1:p.Leu600=
NM_020822.3:c.2308C= MANE Select NP_065873.2:p.Leu770=
NM_001272003.2:c.2173C= NP_001258932.1:p.Leu725=