Canonical Allele Identifier: CA1883884974
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135775401C= , CM000671.2:g.135775401C= GRCh38
NC_000009.11:g.138667247C= , CM000671.1:g.138667247C= GRCh37
NC_000009.10:g.137807068C= NCBI36
NG_033070.1:g.78217C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.2335C= MANE Select ENSP00000360822.2:p.Leu779=
ENST00000674572.1:c.2176C= ENSP00000501742.1:p.Leu726=
ENST00000675090.1:c.2083C= ENSP00000501833.1:p.Leu695=
ENST00000675399.1:c.2083C= ENSP00000501932.1:p.Leu695=
ENST00000676421.1:c.2092C= ENSP00000502322.1:p.Leu698=
ENST00000263604.5:c.2236C= ENSP00000263604.4:p.Leu746=
ENST00000371757.6:c.2335C= ENSP00000360822.2:p.Leu779=
ENST00000460750.5:c.*1945C= ENSP00000418777.1:n.*1945C=
ENST00000486577.6:c.2218C= ENSP00000417578.3:p.Leu740=
ENST00000487664.5:c.2335C= ENSP00000417851.2:p.Leu779=
ENST00000488444.6:c.2278C= ENSP00000419007.3:p.Leu760=
ENST00000490355.6:c.2272C= ENSP00000418003.3:p.Leu758=
ENST00000490363.3:n.2154C=
ENST00000491806.6:c.2278C= ENSP00000419086.3:p.Leu760=
ENST00000628528.2:c.2200C= ENSP00000486374.1:p.Leu734=
ENST00000630792.2:c.2170C= ENSP00000486486.1:p.Leu724=
ENST00000631073.2:c.2278C= ENSP00000486130.1:p.Leu760=
ENST00000631193.1:c.184C= ENSP00000486830.1:p.Leu62=
NM_001272003.1:c.2200C= NP_001258932.1:p.Leu734=
NM_020822.2:c.2335C= NP_065873.2:p.Leu779=
XM_011518877.1:c.2470C= XP_011517179.1:p.Leu824=
XM_011518878.1:c.2479C= XP_011517180.1:p.Leu827=
XM_011518879.1:c.2470C= XP_011517181.1:p.Leu824=
XM_011518880.1:c.2236C= XP_011517182.1:p.Leu746=
XM_011518881.1:c.1825C= XP_011517183.1:p.Leu609=
XM_011518877.3:c.2470C= XP_011517179.1:p.Leu824=
XM_011518878.3:c.2479C= XP_011517180.1:p.Leu827=
XM_011518879.3:c.2470C= XP_011517181.1:p.Leu824=
XM_011518881.3:c.1825C= XP_011517183.1:p.Leu609=
XM_017014931.1:c.2269C= XP_016870420.1:p.Leu757=
XM_017014932.1:c.2092C= XP_016870421.1:p.Leu698=
XM_017014933.1:c.1825C= XP_016870422.1:p.Leu609=
XM_024447617.1:c.1825C= XP_024303385.1:p.Leu609=
XM_024447618.1:c.1825C= XP_024303386.1:p.Leu609=
NM_020822.3:c.2335C= MANE Select NP_065873.2:p.Leu779=
NM_001272003.2:c.2200C= NP_001258932.1:p.Leu734=