Canonical Allele Identifier: CA375512317
Gene: KCNT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135775369A>T , CM000671.2:g.135775369A>T GRCh38
NC_000009.11:g.138667215A>T , CM000671.1:g.138667215A>T GRCh37
NC_000009.10:g.137807036A>T NCBI36
NG_033070.1:g.78185A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.2303A>T MANE Select ENSP00000360822.2:p.His768Leu
ENST00000674572.1:c.2144A>T ENSP00000501742.1:p.His715Leu
ENST00000675090.1:c.2051A>T ENSP00000501833.1:p.His684Leu
ENST00000675399.1:c.2051A>T ENSP00000501932.1:p.His684Leu
ENST00000676421.1:c.2060A>T ENSP00000502322.1:p.His687Leu
ENST00000263604.5:c.2204A>T ENSP00000263604.4:p.His735Leu
ENST00000371757.6:c.2303A>T ENSP00000360822.2:p.His768Leu
ENST00000460750.5:c.*1913A>T ENSP00000418777.1:n.*1913A>T
ENST00000486577.6:c.2186A>T ENSP00000417578.3:p.His729Leu
ENST00000487664.5:c.2303A>T ENSP00000417851.2:p.His768Leu
ENST00000488444.6:c.2246A>T ENSP00000419007.3:p.His749Leu
ENST00000490355.6:c.2240A>T ENSP00000418003.3:p.His747Leu
ENST00000490363.3:n.2122A>T
ENST00000491806.6:c.2246A>T ENSP00000419086.3:p.His749Leu
ENST00000628528.2:c.2168A>T ENSP00000486374.1:p.His723Leu
ENST00000630792.2:c.2138A>T ENSP00000486486.1:p.His713Leu
ENST00000631073.2:c.2246A>T ENSP00000486130.1:p.His749Leu
ENST00000631193.1:c.152A>T ENSP00000486830.1:p.His51Leu
NM_001272003.1:c.2168A>T NP_001258932.1:p.His723Leu
NM_020822.2:c.2303A>T NP_065873.2:p.His768Leu
XM_011518877.1:c.2438A>T XP_011517179.1:p.His813Leu
XM_011518878.1:c.2447A>T XP_011517180.1:p.His816Leu
XM_011518879.1:c.2438A>T XP_011517181.1:p.His813Leu
XM_011518880.1:c.2204A>T XP_011517182.1:p.His735Leu
XM_011518881.1:c.1793A>T XP_011517183.1:p.His598Leu
XM_011518877.3:c.2438A>T XP_011517179.1:p.His813Leu
XM_011518878.3:c.2447A>T XP_011517180.1:p.His816Leu
XM_011518879.3:c.2438A>T XP_011517181.1:p.His813Leu
XM_011518881.3:c.1793A>T XP_011517183.1:p.His598Leu
XM_017014931.1:c.2237A>T XP_016870420.1:p.His746Leu
XM_017014932.1:c.2060A>T XP_016870421.1:p.His687Leu
XM_017014933.1:c.1793A>T XP_016870422.1:p.His598Leu
XM_024447617.1:c.1793A>T XP_024303385.1:p.His598Leu
XM_024447618.1:c.1793A>T XP_024303386.1:p.His598Leu
NM_020822.3:c.2303A>T MANE Select NP_065873.2:p.His768Leu
NM_001272003.2:c.2168A>T NP_001258932.1:p.His723Leu