Canonical Allele Identifier: CA1883872560
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135770027A= , CM000671.2:g.135770027A= GRCh38
NC_000009.11:g.138661873A= , CM000671.1:g.138661873A= GRCh37
NC_000009.10:g.137801694A= NCBI36
NG_033070.1:g.72843A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.1591A= MANE Select ENSP00000360822.2:p.Thr531=
ENST00000674572.1:c.1432A= ENSP00000501742.1:p.Thr478=
ENST00000675090.1:c.1339A= ENSP00000501833.1:p.Thr447=
ENST00000675399.1:c.1339A= ENSP00000501932.1:p.Thr447=
ENST00000676421.1:c.1348A= ENSP00000502322.1:p.Thr450=
ENST00000263604.5:c.1492A= ENSP00000263604.4:p.Thr498=
ENST00000371757.6:c.1591A= ENSP00000360822.2:p.Thr531=
ENST00000460750.5:c.*1201A= ENSP00000418777.1:n.*1201A=
ENST00000486577.6:c.1474A= ENSP00000417578.3:p.Thr492=
ENST00000487664.5:c.1591A= ENSP00000417851.2:p.Thr531=
ENST00000488444.6:c.1534A= ENSP00000419007.3:p.Thr512=
ENST00000490355.6:c.1534A= ENSP00000418003.3:p.Thr512=
ENST00000490363.3:n.1410A=
ENST00000491806.6:c.1534A= ENSP00000419086.3:p.Thr512=
ENST00000628528.2:c.1456A= ENSP00000486374.1:p.Thr486=
ENST00000630792.2:c.1432A= ENSP00000486486.1:p.Thr478=
ENST00000631073.2:c.1534A= ENSP00000486130.1:p.Thr512=
NM_001272003.1:c.1456A= NP_001258932.1:p.Thr486=
NM_020822.2:c.1591A= NP_065873.2:p.Thr531=
XM_011518877.1:c.1726A= XP_011517179.1:p.Thr576=
XM_011518878.1:c.1735A= XP_011517180.1:p.Thr579=
XM_011518879.1:c.1726A= XP_011517181.1:p.Thr576=
XM_011518880.1:c.1492A= XP_011517182.1:p.Thr498=
XM_011518881.1:c.1081A= XP_011517183.1:p.Thr361=
XM_011518877.3:c.1726A= XP_011517179.1:p.Thr576=
XM_011518878.3:c.1735A= XP_011517180.1:p.Thr579=
XM_011518879.3:c.1726A= XP_011517181.1:p.Thr576=
XM_011518881.3:c.1081A= XP_011517183.1:p.Thr361=
XM_017014931.1:c.1525A= XP_016870420.1:p.Thr509=
XM_017014932.1:c.1348A= XP_016870421.1:p.Thr450=
XM_017014933.1:c.1081A= XP_016870422.1:p.Thr361=
XM_024447617.1:c.1081A= XP_024303385.1:p.Thr361=
XM_024447618.1:c.1081A= XP_024303386.1:p.Thr361=
NM_020822.3:c.1591A= MANE Select NP_065873.2:p.Thr531=
NM_001272003.2:c.1456A= NP_001258932.1:p.Thr486=