Canonical Allele Identifier: CA1883884727
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135775336C= , CM000671.2:g.135775336C= GRCh38
NC_000009.11:g.138667182C= , CM000671.1:g.138667182C= GRCh37
NC_000009.10:g.137807003C= NCBI36
NG_033070.1:g.78152C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.2270C= MANE Select ENSP00000360822.2:p.Ser757=
ENST00000674572.1:c.2111C= ENSP00000501742.1:p.Ser704=
ENST00000675090.1:c.2018C= ENSP00000501833.1:p.Ser673=
ENST00000675399.1:c.2018C= ENSP00000501932.1:p.Ser673=
ENST00000676421.1:c.2027C= ENSP00000502322.1:p.Ser676=
ENST00000263604.5:c.2171C= ENSP00000263604.4:p.Ser724=
ENST00000371757.6:c.2270C= ENSP00000360822.2:p.Ser757=
ENST00000460750.5:c.*1880C= ENSP00000418777.1:n.*1880C=
ENST00000486577.6:c.2153C= ENSP00000417578.3:p.Ser718=
ENST00000487664.5:c.2270C= ENSP00000417851.2:p.Ser757=
ENST00000488444.6:c.2213C= ENSP00000419007.3:p.Ser738=
ENST00000490355.6:c.2207C= ENSP00000418003.3:p.Ser736=
ENST00000490363.3:n.2089C=
ENST00000491806.6:c.2213C= ENSP00000419086.3:p.Ser738=
ENST00000628528.2:c.2135C= ENSP00000486374.1:p.Ser712=
ENST00000630792.2:c.2105C= ENSP00000486486.1:p.Ser702=
ENST00000631073.2:c.2213C= ENSP00000486130.1:p.Ser738=
ENST00000631193.1:c.119C= ENSP00000486830.1:p.Ser40=
NM_001272003.1:c.2135C= NP_001258932.1:p.Ser712=
NM_020822.2:c.2270C= NP_065873.2:p.Ser757=
XM_011518877.1:c.2405C= XP_011517179.1:p.Ser802=
XM_011518878.1:c.2414C= XP_011517180.1:p.Ser805=
XM_011518879.1:c.2405C= XP_011517181.1:p.Ser802=
XM_011518880.1:c.2171C= XP_011517182.1:p.Ser724=
XM_011518881.1:c.1760C= XP_011517183.1:p.Ser587=
XM_011518877.3:c.2405C= XP_011517179.1:p.Ser802=
XM_011518878.3:c.2414C= XP_011517180.1:p.Ser805=
XM_011518879.3:c.2405C= XP_011517181.1:p.Ser802=
XM_011518881.3:c.1760C= XP_011517183.1:p.Ser587=
XM_017014931.1:c.2204C= XP_016870420.1:p.Ser735=
XM_017014932.1:c.2027C= XP_016870421.1:p.Ser676=
XM_017014933.1:c.1760C= XP_016870422.1:p.Ser587=
XM_024447617.1:c.1760C= XP_024303385.1:p.Ser587=
XM_024447618.1:c.1760C= XP_024303386.1:p.Ser587=
NM_020822.3:c.2270C= MANE Select NP_065873.2:p.Ser757=
NM_001272003.2:c.2135C= NP_001258932.1:p.Ser712=