Canonical Allele Identifier: CA1883884702
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135775324A= , CM000671.2:g.135775324A= GRCh38
NC_000009.11:g.138667170A= , CM000671.1:g.138667170A= GRCh37
NC_000009.10:g.137806991A= NCBI36
NG_033070.1:g.78140A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.2258A= MANE Select ENSP00000360822.2:p.Tyr753=
ENST00000674572.1:c.2099A= ENSP00000501742.1:p.Tyr700=
ENST00000675090.1:c.2006A= ENSP00000501833.1:p.Tyr669=
ENST00000675399.1:c.2006A= ENSP00000501932.1:p.Tyr669=
ENST00000676421.1:c.2015A= ENSP00000502322.1:p.Tyr672=
ENST00000263604.5:c.2159A= ENSP00000263604.4:p.Tyr720=
ENST00000371757.6:c.2258A= ENSP00000360822.2:p.Tyr753=
ENST00000460750.5:c.*1868A= ENSP00000418777.1:n.*1868A=
ENST00000486577.6:c.2141A= ENSP00000417578.3:p.Tyr714=
ENST00000487664.5:c.2258A= ENSP00000417851.2:p.Tyr753=
ENST00000488444.6:c.2201A= ENSP00000419007.3:p.Tyr734=
ENST00000490355.6:c.2195A= ENSP00000418003.3:p.Tyr732=
ENST00000490363.3:n.2077A=
ENST00000491806.6:c.2201A= ENSP00000419086.3:p.Tyr734=
ENST00000628528.2:c.2123A= ENSP00000486374.1:p.Tyr708=
ENST00000630792.2:c.2093A= ENSP00000486486.1:p.Tyr698=
ENST00000631073.2:c.2201A= ENSP00000486130.1:p.Tyr734=
ENST00000631193.1:c.107A= ENSP00000486830.1:p.Tyr36=
NM_001272003.1:c.2123A= NP_001258932.1:p.Tyr708=
NM_020822.2:c.2258A= NP_065873.2:p.Tyr753=
XM_011518877.1:c.2393A= XP_011517179.1:p.Tyr798=
XM_011518878.1:c.2402A= XP_011517180.1:p.Tyr801=
XM_011518879.1:c.2393A= XP_011517181.1:p.Tyr798=
XM_011518880.1:c.2159A= XP_011517182.1:p.Tyr720=
XM_011518881.1:c.1748A= XP_011517183.1:p.Tyr583=
XM_011518877.3:c.2393A= XP_011517179.1:p.Tyr798=
XM_011518878.3:c.2402A= XP_011517180.1:p.Tyr801=
XM_011518879.3:c.2393A= XP_011517181.1:p.Tyr798=
XM_011518881.3:c.1748A= XP_011517183.1:p.Tyr583=
XM_017014931.1:c.2192A= XP_016870420.1:p.Tyr731=
XM_017014932.1:c.2015A= XP_016870421.1:p.Tyr672=
XM_017014933.1:c.1748A= XP_016870422.1:p.Tyr583=
XM_024447617.1:c.1748A= XP_024303385.1:p.Tyr583=
XM_024447618.1:c.1748A= XP_024303386.1:p.Tyr583=
NM_020822.3:c.2258A= MANE Select NP_065873.2:p.Tyr753=
NM_001272003.2:c.2123A= NP_001258932.1:p.Tyr708=