Canonical Allele Identifier: CA375512150
Gene: KCNT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135775324A>T , CM000671.2:g.135775324A>T GRCh38
NC_000009.11:g.138667170A>T , CM000671.1:g.138667170A>T GRCh37
NC_000009.10:g.137806991A>T NCBI36
NG_033070.1:g.78140A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.2258A>T MANE Select ENSP00000360822.2:p.Tyr753Phe
ENST00000674572.1:c.2099A>T ENSP00000501742.1:p.Tyr700Phe
ENST00000675090.1:c.2006A>T ENSP00000501833.1:p.Tyr669Phe
ENST00000675399.1:c.2006A>T ENSP00000501932.1:p.Tyr669Phe
ENST00000676421.1:c.2015A>T ENSP00000502322.1:p.Tyr672Phe
ENST00000263604.5:c.2159A>T ENSP00000263604.4:p.Tyr720Phe
ENST00000371757.6:c.2258A>T ENSP00000360822.2:p.Tyr753Phe
ENST00000460750.5:c.*1868A>T ENSP00000418777.1:n.*1868A>T
ENST00000486577.6:c.2141A>T ENSP00000417578.3:p.Tyr714Phe
ENST00000487664.5:c.2258A>T ENSP00000417851.2:p.Tyr753Phe
ENST00000488444.6:c.2201A>T ENSP00000419007.3:p.Tyr734Phe
ENST00000490355.6:c.2195A>T ENSP00000418003.3:p.Tyr732Phe
ENST00000490363.3:n.2077A>T
ENST00000491806.6:c.2201A>T ENSP00000419086.3:p.Tyr734Phe
ENST00000628528.2:c.2123A>T ENSP00000486374.1:p.Tyr708Phe
ENST00000630792.2:c.2093A>T ENSP00000486486.1:p.Tyr698Phe
ENST00000631073.2:c.2201A>T ENSP00000486130.1:p.Tyr734Phe
ENST00000631193.1:c.107A>T ENSP00000486830.1:p.Tyr36Phe
NM_001272003.1:c.2123A>T NP_001258932.1:p.Tyr708Phe
NM_020822.2:c.2258A>T NP_065873.2:p.Tyr753Phe
XM_011518877.1:c.2393A>T XP_011517179.1:p.Tyr798Phe
XM_011518878.1:c.2402A>T XP_011517180.1:p.Tyr801Phe
XM_011518879.1:c.2393A>T XP_011517181.1:p.Tyr798Phe
XM_011518880.1:c.2159A>T XP_011517182.1:p.Tyr720Phe
XM_011518881.1:c.1748A>T XP_011517183.1:p.Tyr583Phe
XM_011518877.3:c.2393A>T XP_011517179.1:p.Tyr798Phe
XM_011518878.3:c.2402A>T XP_011517180.1:p.Tyr801Phe
XM_011518879.3:c.2393A>T XP_011517181.1:p.Tyr798Phe
XM_011518881.3:c.1748A>T XP_011517183.1:p.Tyr583Phe
XM_017014931.1:c.2192A>T XP_016870420.1:p.Tyr731Phe
XM_017014932.1:c.2015A>T XP_016870421.1:p.Tyr672Phe
XM_017014933.1:c.1748A>T XP_016870422.1:p.Tyr583Phe
XM_024447617.1:c.1748A>T XP_024303385.1:p.Tyr583Phe
XM_024447618.1:c.1748A>T XP_024303386.1:p.Tyr583Phe
NM_020822.3:c.2258A>T MANE Select NP_065873.2:p.Tyr753Phe
NM_001272003.2:c.2123A>T NP_001258932.1:p.Tyr708Phe