Canonical Allele Identifier: CA1883873234
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135770299G= , CM000671.2:g.135770299G= GRCh38
NC_000009.11:g.138662145G= , CM000671.1:g.138662145G= GRCh37
NC_000009.10:g.137801966G= NCBI36
NG_033070.1:g.73115G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.1621G= MANE Select ENSP00000360822.2:p.Glu541=
ENST00000674572.1:c.1462G= ENSP00000501742.1:p.Glu488=
ENST00000675090.1:c.1369G= ENSP00000501833.1:p.Glu457=
ENST00000675399.1:c.1369G= ENSP00000501932.1:p.Glu457=
ENST00000676421.1:c.1378G= ENSP00000502322.1:p.Glu460=
ENST00000263604.5:c.1522G= ENSP00000263604.4:p.Glu508=
ENST00000371757.6:c.1621G= ENSP00000360822.2:p.Glu541=
ENST00000460750.5:c.*1231G= ENSP00000418777.1:n.*1231G=
ENST00000486577.6:c.1504G= ENSP00000417578.3:p.Glu502=
ENST00000487664.5:c.1621G= ENSP00000417851.2:p.Glu541=
ENST00000488444.6:c.1564G= ENSP00000419007.3:p.Glu522=
ENST00000490355.6:c.1564G= ENSP00000418003.3:p.Glu522=
ENST00000490363.3:n.1440G=
ENST00000491806.6:c.1564G= ENSP00000419086.3:p.Glu522=
ENST00000628528.2:c.1486G= ENSP00000486374.1:p.Glu496=
ENST00000630792.2:c.1462G= ENSP00000486486.1:p.Glu488=
ENST00000631073.2:c.1564G= ENSP00000486130.1:p.Glu522=
NM_001272003.1:c.1486G= NP_001258932.1:p.Glu496=
NM_020822.2:c.1621G= NP_065873.2:p.Glu541=
XM_011518877.1:c.1756G= XP_011517179.1:p.Glu586=
XM_011518878.1:c.1765G= XP_011517180.1:p.Glu589=
XM_011518879.1:c.1756G= XP_011517181.1:p.Glu586=
XM_011518880.1:c.1522G= XP_011517182.1:p.Glu508=
XM_011518881.1:c.1111G= XP_011517183.1:p.Glu371=
XM_011518877.3:c.1756G= XP_011517179.1:p.Glu586=
XM_011518878.3:c.1765G= XP_011517180.1:p.Glu589=
XM_011518879.3:c.1756G= XP_011517181.1:p.Glu586=
XM_011518881.3:c.1111G= XP_011517183.1:p.Glu371=
XM_017014931.1:c.1555G= XP_016870420.1:p.Glu519=
XM_017014932.1:c.1378G= XP_016870421.1:p.Glu460=
XM_017014933.1:c.1111G= XP_016870422.1:p.Glu371=
XM_024447617.1:c.1111G= XP_024303385.1:p.Glu371=
XM_024447618.1:c.1111G= XP_024303386.1:p.Glu371=
NM_020822.3:c.1621G= MANE Select NP_065873.2:p.Glu541=
NM_001272003.2:c.1486G= NP_001258932.1:p.Glu496=