Canonical Allele Identifier: CA1883892496
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135791838A= , CM000671.2:g.135791838A= GRCh38
NC_000009.11:g.138683684A= , CM000671.1:g.138683684A= GRCh37
NC_000009.10:g.137823505A= NCBI36
NG_033070.1:g.94654A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.3544A= MANE Select ENSP00000360822.2:p.Ile1182=
ENST00000674572.1:c.3448A= ENSP00000501742.1:p.Ile1150=
ENST00000675090.1:c.3292A= ENSP00000501833.1:p.Ile1098=
ENST00000675399.1:c.3355A= ENSP00000501932.1:p.Ile1119=
ENST00000676421.1:c.3364A= ENSP00000502322.1:p.Ile1122=
ENST00000263604.5:c.3508A= ENSP00000263604.4:p.Ile1170=
ENST00000371757.6:c.3544A= ENSP00000360822.2:p.Ile1182=
ENST00000460750.5:c.*3217A= ENSP00000418777.1:n.*3217A=
ENST00000475008.1:n.2850A=
ENST00000486577.6:c.3490A= ENSP00000417578.3:p.Ile1164=
ENST00000487664.5:c.3607A= ENSP00000417851.2:p.Ile1203=
ENST00000488444.6:c.3529A= ENSP00000419007.3:p.Ile1177=
ENST00000490355.6:c.3544A= ENSP00000418003.3:p.Ile1182=
ENST00000491806.6:c.3487A= ENSP00000419086.3:p.Ile1163=
ENST00000628528.2:c.3472A= ENSP00000486374.1:p.Ile1158=
ENST00000630792.2:c.3442A= ENSP00000486486.1:p.Ile1148=
ENST00000631073.2:c.3550A= ENSP00000486130.1:p.Ile1184=
NM_001272003.1:c.3472A= NP_001258932.1:p.Ile1158=
NM_020822.2:c.3544A= NP_065873.2:p.Ile1182=
XM_011518877.1:c.3742A= XP_011517179.1:p.Ile1248=
XM_011518878.1:c.3688A= XP_011517180.1:p.Ile1230=
XM_011518879.1:c.3679A= XP_011517181.1:p.Ile1227=
XM_011518880.1:c.3508A= XP_011517182.1:p.Ile1170=
XM_011518881.1:c.3097A= XP_011517183.1:p.Ile1033=
XM_011518877.3:c.3742A= XP_011517179.1:p.Ile1248=
XM_011518878.3:c.3688A= XP_011517180.1:p.Ile1230=
XM_011518879.3:c.3679A= XP_011517181.1:p.Ile1227=
XM_011518881.3:c.3097A= XP_011517183.1:p.Ile1033=
XM_017014931.1:c.3541A= XP_016870420.1:p.Ile1181=
XM_017014932.1:c.3364A= XP_016870421.1:p.Ile1122=
XM_017014933.1:c.3097A= XP_016870422.1:p.Ile1033=
XM_024447617.1:c.3097A= XP_024303385.1:p.Ile1033=
XM_024447618.1:c.3097A= XP_024303386.1:p.Ile1033=
NM_020822.3:c.3544A= MANE Select NP_065873.2:p.Ile1182=
NM_001272003.2:c.3472A= NP_001258932.1:p.Ile1158=