Canonical Allele Identifier: CA1883872550
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135770021C= , CM000671.2:g.135770021C= GRCh38
NC_000009.11:g.138661867C= , CM000671.1:g.138661867C= GRCh37
NC_000009.10:g.137801688C= NCBI36
NG_033070.1:g.72837C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.1585C= MANE Select ENSP00000360822.2:p.Leu529=
ENST00000674572.1:c.1426C= ENSP00000501742.1:p.Leu476=
ENST00000675090.1:c.1333C= ENSP00000501833.1:p.Leu445=
ENST00000675399.1:c.1333C= ENSP00000501932.1:p.Leu445=
ENST00000676421.1:c.1342C= ENSP00000502322.1:p.Leu448=
ENST00000263604.5:c.1486C= ENSP00000263604.4:p.Leu496=
ENST00000371757.6:c.1585C= ENSP00000360822.2:p.Leu529=
ENST00000460750.5:c.*1195C= ENSP00000418777.1:n.*1195C=
ENST00000486577.6:c.1468C= ENSP00000417578.3:p.Leu490=
ENST00000487664.5:c.1585C= ENSP00000417851.2:p.Leu529=
ENST00000488444.6:c.1528C= ENSP00000419007.3:p.Leu510=
ENST00000490355.6:c.1528C= ENSP00000418003.3:p.Leu510=
ENST00000490363.3:n.1404C=
ENST00000491806.6:c.1528C= ENSP00000419086.3:p.Leu510=
ENST00000628528.2:c.1450C= ENSP00000486374.1:p.Leu484=
ENST00000630792.2:c.1426C= ENSP00000486486.1:p.Leu476=
ENST00000631073.2:c.1528C= ENSP00000486130.1:p.Leu510=
NM_001272003.1:c.1450C= NP_001258932.1:p.Leu484=
NM_020822.2:c.1585C= NP_065873.2:p.Leu529=
XM_011518877.1:c.1720C= XP_011517179.1:p.Leu574=
XM_011518878.1:c.1729C= XP_011517180.1:p.Leu577=
XM_011518879.1:c.1720C= XP_011517181.1:p.Leu574=
XM_011518880.1:c.1486C= XP_011517182.1:p.Leu496=
XM_011518881.1:c.1075C= XP_011517183.1:p.Leu359=
XM_011518877.3:c.1720C= XP_011517179.1:p.Leu574=
XM_011518878.3:c.1729C= XP_011517180.1:p.Leu577=
XM_011518879.3:c.1720C= XP_011517181.1:p.Leu574=
XM_011518881.3:c.1075C= XP_011517183.1:p.Leu359=
XM_017014931.1:c.1519C= XP_016870420.1:p.Leu507=
XM_017014932.1:c.1342C= XP_016870421.1:p.Leu448=
XM_017014933.1:c.1075C= XP_016870422.1:p.Leu359=
XM_024447617.1:c.1075C= XP_024303385.1:p.Leu359=
XM_024447618.1:c.1075C= XP_024303386.1:p.Leu359=
NM_020822.3:c.1585C= MANE Select NP_065873.2:p.Leu529=
NM_001272003.2:c.1450C= NP_001258932.1:p.Leu484=