Canonical Allele Identifier: CA1883888302
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135786419A= , CM000671.2:g.135786419A= GRCh38
NC_000009.11:g.138678265A= , CM000671.1:g.138678265A= GRCh37
NC_000009.10:g.137818086A= NCBI36
NG_033070.1:g.89235A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371757.7:c.3400A= MANE Select ENSP00000360822.2:p.Ser1134=
ENST00000674572.1:c.3241A= ENSP00000501742.1:p.Ser1081=
ENST00000675090.1:c.3148A= ENSP00000501833.1:p.Ser1050=
ENST00000675399.1:c.3148A= ENSP00000501932.1:p.Ser1050=
ENST00000676421.1:c.3157A= ENSP00000502322.1:p.Ser1053=
ENST00000263604.5:c.3301A= ENSP00000263604.4:p.Ser1101=
ENST00000371757.6:c.3400A= ENSP00000360822.2:p.Ser1134=
ENST00000460750.5:c.*3010A= ENSP00000418777.1:n.*3010A=
ENST00000486577.6:c.3283A= ENSP00000417578.3:p.Ser1095=
ENST00000487664.5:c.3400A= ENSP00000417851.2:p.Ser1134=
ENST00000488444.6:c.3322A= ENSP00000419007.3:p.Ser1108=
ENST00000490355.6:c.3337A= ENSP00000418003.3:p.Ser1113=
ENST00000491806.6:c.3343A= ENSP00000419086.3:p.Ser1115=
ENST00000628528.2:c.3265A= ENSP00000486374.1:p.Ser1089=
ENST00000630792.2:c.3235A= ENSP00000486486.1:p.Ser1079=
ENST00000631073.2:c.3343A= ENSP00000486130.1:p.Ser1115=
NM_001272003.1:c.3265A= NP_001258932.1:p.Ser1089=
NM_020822.2:c.3400A= NP_065873.2:p.Ser1134=
XM_011518877.1:c.3535A= XP_011517179.1:p.Ser1179=
XM_011518878.1:c.3544A= XP_011517180.1:p.Ser1182=
XM_011518879.1:c.3535A= XP_011517181.1:p.Ser1179=
XM_011518880.1:c.3301A= XP_011517182.1:p.Ser1101=
XM_011518881.1:c.2890A= XP_011517183.1:p.Ser964=
XM_011518877.3:c.3535A= XP_011517179.1:p.Ser1179=
XM_011518878.3:c.3544A= XP_011517180.1:p.Ser1182=
XM_011518879.3:c.3535A= XP_011517181.1:p.Ser1179=
XM_011518881.3:c.2890A= XP_011517183.1:p.Ser964=
XM_017014931.1:c.3334A= XP_016870420.1:p.Ser1112=
XM_017014932.1:c.3157A= XP_016870421.1:p.Ser1053=
XM_017014933.1:c.2890A= XP_016870422.1:p.Ser964=
XM_024447617.1:c.2890A= XP_024303385.1:p.Ser964=
XM_024447618.1:c.2890A= XP_024303386.1:p.Ser964=
NM_020822.3:c.3400A= MANE Select NP_065873.2:p.Ser1134=
NM_001272003.2:c.3265A= NP_001258932.1:p.Ser1089=