Canonical Allele Identifier: CA375506026
Gene: KCNT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135770040A>T , CM000671.2:g.135770040A>T GRCh38
NC_000009.11:g.138661886A>T , CM000671.1:g.138661886A>T GRCh37
NC_000009.10:g.137801707A>T NCBI36
NG_033070.1:g.72856A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.1604A>T MANE Select ENSP00000360822.2:p.His535Leu
ENST00000674572.1:c.1445A>T ENSP00000501742.1:p.His482Leu
ENST00000675090.1:c.1352A>T ENSP00000501833.1:p.His451Leu
ENST00000675399.1:c.1352A>T ENSP00000501932.1:p.His451Leu
ENST00000676421.1:c.1361A>T ENSP00000502322.1:p.His454Leu
ENST00000263604.5:c.1505A>T ENSP00000263604.4:p.His502Leu
ENST00000371757.6:c.1604A>T ENSP00000360822.2:p.His535Leu
ENST00000460750.5:c.*1214A>T ENSP00000418777.1:n.*1214A>T
ENST00000486577.6:c.1487A>T ENSP00000417578.3:p.His496Leu
ENST00000487664.5:c.1604A>T ENSP00000417851.2:p.His535Leu
ENST00000488444.6:c.1547A>T ENSP00000419007.3:p.His516Leu
ENST00000490355.6:c.1547A>T ENSP00000418003.3:p.His516Leu
ENST00000490363.3:n.1423A>T
ENST00000491806.6:c.1547A>T ENSP00000419086.3:p.His516Leu
ENST00000628528.2:c.1469A>T ENSP00000486374.1:p.His490Leu
ENST00000630792.2:c.1445A>T ENSP00000486486.1:p.His482Leu
ENST00000631073.2:c.1547A>T ENSP00000486130.1:p.His516Leu
NM_001272003.1:c.1469A>T NP_001258932.1:p.His490Leu
NM_020822.2:c.1604A>T NP_065873.2:p.His535Leu
XM_011518877.1:c.1739A>T XP_011517179.1:p.His580Leu
XM_011518878.1:c.1748A>T XP_011517180.1:p.His583Leu
XM_011518879.1:c.1739A>T XP_011517181.1:p.His580Leu
XM_011518880.1:c.1505A>T XP_011517182.1:p.His502Leu
XM_011518881.1:c.1094A>T XP_011517183.1:p.His365Leu
XM_011518877.3:c.1739A>T XP_011517179.1:p.His580Leu
XM_011518878.3:c.1748A>T XP_011517180.1:p.His583Leu
XM_011518879.3:c.1739A>T XP_011517181.1:p.His580Leu
XM_011518881.3:c.1094A>T XP_011517183.1:p.His365Leu
XM_017014931.1:c.1538A>T XP_016870420.1:p.His513Leu
XM_017014932.1:c.1361A>T XP_016870421.1:p.His454Leu
XM_017014933.1:c.1094A>T XP_016870422.1:p.His365Leu
XM_024447617.1:c.1094A>T XP_024303385.1:p.His365Leu
XM_024447618.1:c.1094A>T XP_024303386.1:p.His365Leu
NM_020822.3:c.1604A>T MANE Select NP_065873.2:p.His535Leu
NM_001272003.2:c.1469A>T NP_001258932.1:p.His490Leu