Canonical Allele Identifier: CA1883866825
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135765930_135765958delinsCGGGGTGGACCATTTAGGGTGGATCGTCT , CM000671.2:g.135765930_135765958delinsCGGGGTGGACCATTTAGGGTGGATCGTCT GRCh38
NC_000009.11:g.138657776_138657804delinsCGGGGTGGACCATTTAGGGTGGATCGTCT , CM000671.1:g.138657776_138657804delinsCGGGGTGGACCATTTAGGGTGGATCGTCT GRCh37
NC_000009.10:g.137797597_137797625delinsCGGGGTGGACCATTTAGGGTGGATCGTCT NCBI36
NG_033070.1:g.68746_68774delinsCGGGGTGGACCATTTAGGGTGGATCGTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.1337+170_1337+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT MANE Select ENSP00000360822.2:n.1337+170_1337+198delinsCGGGGTGGACCATTTAGG...
ENST00000636003.1:c.27+170_27+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT
ENST00000636995.1:n.64+170_64+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT
ENST00000637798.1:n.76+170_76+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT
ENST00000674572.1:c.1178+170_1178+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000501742.1:n.1178+170_1178+198delinsCGGGGTGGACCATTTAGG...
ENST00000675090.1:c.1085+170_1085+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000501833.1:n.1085+170_1085+198delinsCGGGGTGGACCATTTAGG...
ENST00000675399.1:c.1085+170_1085+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000501932.1:n.1085+170_1085+198delinsCGGGGTGGACCATTTAGG...
ENST00000676421.1:c.1094+170_1094+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000502322.1:n.1094+170_1094+198delinsCGGGGTGGACCATTTAGG...
ENST00000263604.5:c.1238+170_1238+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000263604.4:n.1238+170_1238+198delinsCGGGGTGGACCATTTAGG...
ENST00000371757.6:c.1337+170_1337+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000360822.2:n.1337+170_1337+198delinsCGGGGTGGACCATTTAGG...
ENST00000460750.5:c.*947+170_*947+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000418777.1:n.*947+170_*947+198delinsCGGGGTGGACCATTTAGG...
ENST00000486577.6:c.1220+170_1220+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000417578.3:n.1220+170_1220+198delinsCGGGGTGGACCATTTAGG...
ENST00000487664.5:c.1337+170_1337+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000417851.2:n.1337+170_1337+198delinsCGGGGTGGACCATTTAGG...
ENST00000488444.6:c.1280+170_1280+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000419007.3:n.1280+170_1280+198delinsCGGGGTGGACCATTTAGG...
ENST00000490355.6:c.1280+170_1280+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000418003.3:n.1280+170_1280+198delinsCGGGGTGGACCATTTAGG...
ENST00000490363.3:n.1156+170_1156+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT
ENST00000491806.6:c.1280+170_1280+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000419086.3:n.1280+170_1280+198delinsCGGGGTGGACCATTTAGG...
ENST00000628528.2:c.1202+170_1202+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000486374.1:n.1202+170_1202+198delinsCGGGGTGGACCATTTAGG...
ENST00000630792.2:c.1178+170_1178+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000486486.1:n.1178+170_1178+198delinsCGGGGTGGACCATTTAGG...
ENST00000631073.2:c.1280+170_1280+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT ENSP00000486130.1:n.1280+170_1280+198delinsCGGGGTGGACCATTTAGG...
NM_001272003.1:c.1202+170_1202+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT NP_001258932.1:n.1202+170_1202+198delinsCGGGGTGGACCATTTAGGGTG...
NM_020822.2:c.1337+170_1337+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT NP_065873.2:n.1337+170_1337+198delinsCGGGGTGGACCATTTAGGGTGGAT...
XM_011518877.1:c.1472+170_1472+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_011517179.1:n.1472+170_1472+198delinsCGGGGTGGACCATTTAGGGTG...
XM_011518878.1:c.1481+170_1481+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_011517180.1:n.1481+170_1481+198delinsCGGGGTGGACCATTTAGGGTG...
XM_011518879.1:c.1472+170_1472+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_011517181.1:n.1472+170_1472+198delinsCGGGGTGGACCATTTAGGGTG...
XM_011518880.1:c.1238+170_1238+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_011517182.1:n.1238+170_1238+198delinsCGGGGTGGACCATTTAGGGTG...
XM_011518881.1:c.827+170_827+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_011517183.1:n.827+170_827+198delinsCGGGGTGGACCATTTAGGGTGGA...
XM_011518877.3:c.1472+170_1472+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_011517179.1:n.1472+170_1472+198delinsCGGGGTGGACCATTTAGGGTG...
XM_011518878.3:c.1481+170_1481+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_011517180.1:n.1481+170_1481+198delinsCGGGGTGGACCATTTAGGGTG...
XM_011518879.3:c.1472+170_1472+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_011517181.1:n.1472+170_1472+198delinsCGGGGTGGACCATTTAGGGTG...
XM_011518881.3:c.827+170_827+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_011517183.1:n.827+170_827+198delinsCGGGGTGGACCATTTAGGGTGGA...
XM_017014931.1:c.1271+170_1271+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_016870420.1:n.1271+170_1271+198delinsCGGGGTGGACCATTTAGGGTG...
XM_017014932.1:c.1094+170_1094+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_016870421.1:n.1094+170_1094+198delinsCGGGGTGGACCATTTAGGGTG...
XM_017014933.1:c.827+170_827+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_016870422.1:n.827+170_827+198delinsCGGGGTGGACCATTTAGGGTGGA...
XM_024447617.1:c.827+170_827+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_024303385.1:n.827+170_827+198delinsCGGGGTGGACCATTTAGGGTGGA...
XM_024447618.1:c.827+170_827+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT XP_024303386.1:n.827+170_827+198delinsCGGGGTGGACCATTTAGGGTGGA...
NM_020822.3:c.1337+170_1337+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT MANE Select NP_065873.2:n.1337+170_1337+198delinsCGGGGTGGACCATTTAGGGTGGAT...
NM_001272003.2:c.1202+170_1202+198delinsCGGGGTGGACCATTTAGGGTGGATCGTCT NP_001258932.1:n.1202+170_1202+198delinsCGGGGTGGACCATTTAGGGTG...