Canonical Allele Identifier: CA1883866686
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135765700C= , CM000671.2:g.135765700C= GRCh38
NC_000009.11:g.138657546C= , CM000671.1:g.138657546C= GRCh37
NC_000009.10:g.137797367C= NCBI36
NG_033070.1:g.68516C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.1277C= MANE Select ENSP00000360822.2:p.Ser426=
ENST00000636995.1:n.4C=
ENST00000637798.1:n.16C=
ENST00000674572.1:c.1118C= ENSP00000501742.1:p.Ser373=
ENST00000675090.1:c.1025C= ENSP00000501833.1:p.Ser342=
ENST00000675399.1:c.1025C= ENSP00000501932.1:p.Ser342=
ENST00000676421.1:c.1034C= ENSP00000502322.1:p.Ser345=
ENST00000263604.5:c.1178C= ENSP00000263604.4:p.Ser393=
ENST00000371757.6:c.1277C= ENSP00000360822.2:p.Ser426=
ENST00000460750.5:c.*887C= ENSP00000418777.1:n.*887C=
ENST00000486577.6:c.1160C= ENSP00000417578.3:p.Ser387=
ENST00000487664.5:c.1277C= ENSP00000417851.2:p.Ser426=
ENST00000488444.6:c.1220C= ENSP00000419007.3:p.Ser407=
ENST00000490355.6:c.1220C= ENSP00000418003.3:p.Ser407=
ENST00000490363.3:n.1096C=
ENST00000491806.6:c.1220C= ENSP00000419086.3:p.Ser407=
ENST00000628528.2:c.1142C= ENSP00000486374.1:p.Ser381=
ENST00000630792.2:c.1118C= ENSP00000486486.1:p.Ser373=
ENST00000631073.2:c.1220C= ENSP00000486130.1:p.Ser407=
NM_001272003.1:c.1142C= NP_001258932.1:p.Ser381=
NM_020822.2:c.1277C= NP_065873.2:p.Ser426=
XM_011518877.1:c.1412C= XP_011517179.1:p.Ser471=
XM_011518878.1:c.1421C= XP_011517180.1:p.Ser474=
XM_011518879.1:c.1412C= XP_011517181.1:p.Ser471=
XM_011518880.1:c.1178C= XP_011517182.1:p.Ser393=
XM_011518881.1:c.767C= XP_011517183.1:p.Ser256=
XM_011518877.3:c.1412C= XP_011517179.1:p.Ser471=
XM_011518878.3:c.1421C= XP_011517180.1:p.Ser474=
XM_011518879.3:c.1412C= XP_011517181.1:p.Ser471=
XM_011518881.3:c.767C= XP_011517183.1:p.Ser256=
XM_017014931.1:c.1211C= XP_016870420.1:p.Ser404=
XM_017014932.1:c.1034C= XP_016870421.1:p.Ser345=
XM_017014933.1:c.767C= XP_016870422.1:p.Ser256=
XM_024447617.1:c.767C= XP_024303385.1:p.Ser256=
XM_024447618.1:c.767C= XP_024303386.1:p.Ser256=
NM_020822.3:c.1277C= MANE Select NP_065873.2:p.Ser426=
NM_001272003.2:c.1142C= NP_001258932.1:p.Ser381=