Canonical Allele Identifier: CA1883884960
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135775394C= , CM000671.2:g.135775394C= GRCh38
NC_000009.11:g.138667240C= , CM000671.1:g.138667240C= GRCh37
NC_000009.10:g.137807061C= NCBI36
NG_033070.1:g.78210C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.2328C= MANE Select ENSP00000360822.2:p.Phe776=
ENST00000674572.1:c.2169C= ENSP00000501742.1:p.Phe723=
ENST00000675090.1:c.2076C= ENSP00000501833.1:p.Phe692=
ENST00000675399.1:c.2076C= ENSP00000501932.1:p.Phe692=
ENST00000676421.1:c.2085C= ENSP00000502322.1:p.Phe695=
ENST00000263604.5:c.2229C= ENSP00000263604.4:p.Phe743=
ENST00000371757.6:c.2328C= ENSP00000360822.2:p.Phe776=
ENST00000460750.5:c.*1938C= ENSP00000418777.1:n.*1938C=
ENST00000486577.6:c.2211C= ENSP00000417578.3:p.Phe737=
ENST00000487664.5:c.2328C= ENSP00000417851.2:p.Phe776=
ENST00000488444.6:c.2271C= ENSP00000419007.3:p.Phe757=
ENST00000490355.6:c.2265C= ENSP00000418003.3:p.Phe755=
ENST00000490363.3:n.2147C=
ENST00000491806.6:c.2271C= ENSP00000419086.3:p.Phe757=
ENST00000628528.2:c.2193C= ENSP00000486374.1:p.Phe731=
ENST00000630792.2:c.2163C= ENSP00000486486.1:p.Phe721=
ENST00000631073.2:c.2271C= ENSP00000486130.1:p.Phe757=
ENST00000631193.1:c.177C= ENSP00000486830.1:p.Phe59=
NM_001272003.1:c.2193C= NP_001258932.1:p.Phe731=
NM_020822.2:c.2328C= NP_065873.2:p.Phe776=
XM_011518877.1:c.2463C= XP_011517179.1:p.Phe821=
XM_011518878.1:c.2472C= XP_011517180.1:p.Phe824=
XM_011518879.1:c.2463C= XP_011517181.1:p.Phe821=
XM_011518880.1:c.2229C= XP_011517182.1:p.Phe743=
XM_011518881.1:c.1818C= XP_011517183.1:p.Phe606=
XM_011518877.3:c.2463C= XP_011517179.1:p.Phe821=
XM_011518878.3:c.2472C= XP_011517180.1:p.Phe824=
XM_011518879.3:c.2463C= XP_011517181.1:p.Phe821=
XM_011518881.3:c.1818C= XP_011517183.1:p.Phe606=
XM_017014931.1:c.2262C= XP_016870420.1:p.Phe754=
XM_017014932.1:c.2085C= XP_016870421.1:p.Phe695=
XM_017014933.1:c.1818C= XP_016870422.1:p.Phe606=
XM_024447617.1:c.1818C= XP_024303385.1:p.Phe606=
XM_024447618.1:c.1818C= XP_024303386.1:p.Phe606=
NM_020822.3:c.2328C= MANE Select NP_065873.2:p.Phe776=
NM_001272003.2:c.2193C= NP_001258932.1:p.Phe731=