Canonical Allele Identifier: CA1883884746
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135775339C= , CM000671.2:g.135775339C= GRCh38
NC_000009.11:g.138667185C= , CM000671.1:g.138667185C= GRCh37
NC_000009.10:g.137807006C= NCBI36
NG_033070.1:g.78155C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.2273C= MANE Select ENSP00000360822.2:p.Pro758=
ENST00000674572.1:c.2114C= ENSP00000501742.1:p.Pro705=
ENST00000675090.1:c.2021C= ENSP00000501833.1:p.Pro674=
ENST00000675399.1:c.2021C= ENSP00000501932.1:p.Pro674=
ENST00000676421.1:c.2030C= ENSP00000502322.1:p.Pro677=
ENST00000263604.5:c.2174C= ENSP00000263604.4:p.Pro725=
ENST00000371757.6:c.2273C= ENSP00000360822.2:p.Pro758=
ENST00000460750.5:c.*1883C= ENSP00000418777.1:n.*1883C=
ENST00000486577.6:c.2156C= ENSP00000417578.3:p.Pro719=
ENST00000487664.5:c.2273C= ENSP00000417851.2:p.Pro758=
ENST00000488444.6:c.2216C= ENSP00000419007.3:p.Pro739=
ENST00000490355.6:c.2210C= ENSP00000418003.3:p.Pro737=
ENST00000490363.3:n.2092C=
ENST00000491806.6:c.2216C= ENSP00000419086.3:p.Pro739=
ENST00000628528.2:c.2138C= ENSP00000486374.1:p.Pro713=
ENST00000630792.2:c.2108C= ENSP00000486486.1:p.Pro703=
ENST00000631073.2:c.2216C= ENSP00000486130.1:p.Pro739=
ENST00000631193.1:c.122C= ENSP00000486830.1:p.Pro41=
NM_001272003.1:c.2138C= NP_001258932.1:p.Pro713=
NM_020822.2:c.2273C= NP_065873.2:p.Pro758=
XM_011518877.1:c.2408C= XP_011517179.1:p.Pro803=
XM_011518878.1:c.2417C= XP_011517180.1:p.Pro806=
XM_011518879.1:c.2408C= XP_011517181.1:p.Pro803=
XM_011518880.1:c.2174C= XP_011517182.1:p.Pro725=
XM_011518881.1:c.1763C= XP_011517183.1:p.Pro588=
XM_011518877.3:c.2408C= XP_011517179.1:p.Pro803=
XM_011518878.3:c.2417C= XP_011517180.1:p.Pro806=
XM_011518879.3:c.2408C= XP_011517181.1:p.Pro803=
XM_011518881.3:c.1763C= XP_011517183.1:p.Pro588=
XM_017014931.1:c.2207C= XP_016870420.1:p.Pro736=
XM_017014932.1:c.2030C= XP_016870421.1:p.Pro677=
XM_017014933.1:c.1763C= XP_016870422.1:p.Pro588=
XM_024447617.1:c.1763C= XP_024303385.1:p.Pro588=
XM_024447618.1:c.1763C= XP_024303386.1:p.Pro588=
NM_020822.3:c.2273C= MANE Select NP_065873.2:p.Pro758=
NM_001272003.2:c.2138C= NP_001258932.1:p.Pro713=