Canonical Allele Identifier: CA1883866816

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765916_135765944delinsCAGGGTGGATCGTCCGGGGTGGACCATTT , CM000671.2:g.135765916_135765944delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	GRCh38
NC_000009.11:g.138657762_138657790delinsCAGGGTGGATCGTCCGGGGTGGACCATTT , CM000671.1:g.138657762_138657790delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	GRCh37
NC_000009.10:g.137797583_137797611delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	NCBI36
NG_033070.1:g.68732_68760delinsCAGGGTGGATCGTCCGGGGTGGACCATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1337+156_1337+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT MANE Select	ENSP00000360822.2:n.1337+156_1337+184delinsCAGGGTGGATCGTCCGGG...
ENST00000636003.1:c.27+156_27+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT
ENST00000636995.1:n.64+156_64+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT
ENST00000637798.1:n.76+156_76+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT
ENST00000674572.1:c.1178+156_1178+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000501742.1:n.1178+156_1178+184delinsCAGGGTGGATCGTCCGGG...
ENST00000675090.1:c.1085+156_1085+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000501833.1:n.1085+156_1085+184delinsCAGGGTGGATCGTCCGGG...
ENST00000675399.1:c.1085+156_1085+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000501932.1:n.1085+156_1085+184delinsCAGGGTGGATCGTCCGGG...
ENST00000676421.1:c.1094+156_1094+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000502322.1:n.1094+156_1094+184delinsCAGGGTGGATCGTCCGGG...
ENST00000263604.5:c.1238+156_1238+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000263604.4:n.1238+156_1238+184delinsCAGGGTGGATCGTCCGGG...
ENST00000371757.6:c.1337+156_1337+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000360822.2:n.1337+156_1337+184delinsCAGGGTGGATCGTCCGGG...
ENST00000460750.5:c.*947+156_*947+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000418777.1:n.*947+156_*947+184delinsCAGGGTGGATCGTCCGGG...
ENST00000486577.6:c.1220+156_1220+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000417578.3:n.1220+156_1220+184delinsCAGGGTGGATCGTCCGGG...
ENST00000487664.5:c.1337+156_1337+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000417851.2:n.1337+156_1337+184delinsCAGGGTGGATCGTCCGGG...
ENST00000488444.6:c.1280+156_1280+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000419007.3:n.1280+156_1280+184delinsCAGGGTGGATCGTCCGGG...
ENST00000490355.6:c.1280+156_1280+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000418003.3:n.1280+156_1280+184delinsCAGGGTGGATCGTCCGGG...
ENST00000490363.3:n.1156+156_1156+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT
ENST00000491806.6:c.1280+156_1280+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000419086.3:n.1280+156_1280+184delinsCAGGGTGGATCGTCCGGG...
ENST00000628528.2:c.1202+156_1202+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000486374.1:n.1202+156_1202+184delinsCAGGGTGGATCGTCCGGG...
ENST00000630792.2:c.1178+156_1178+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000486486.1:n.1178+156_1178+184delinsCAGGGTGGATCGTCCGGG...
ENST00000631073.2:c.1280+156_1280+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	ENSP00000486130.1:n.1280+156_1280+184delinsCAGGGTGGATCGTCCGGG...
NM_001272003.1:c.1202+156_1202+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	NP_001258932.1:n.1202+156_1202+184delinsCAGGGTGGATCGTCCGGGGTG...
NM_020822.2:c.1337+156_1337+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	NP_065873.2:n.1337+156_1337+184delinsCAGGGTGGATCGTCCGGGGTGGAC...
XM_011518877.1:c.1472+156_1472+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_011517179.1:n.1472+156_1472+184delinsCAGGGTGGATCGTCCGGGGTG...
XM_011518878.1:c.1481+156_1481+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_011517180.1:n.1481+156_1481+184delinsCAGGGTGGATCGTCCGGGGTG...
XM_011518879.1:c.1472+156_1472+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_011517181.1:n.1472+156_1472+184delinsCAGGGTGGATCGTCCGGGGTG...
XM_011518880.1:c.1238+156_1238+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_011517182.1:n.1238+156_1238+184delinsCAGGGTGGATCGTCCGGGGTG...
XM_011518881.1:c.827+156_827+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_011517183.1:n.827+156_827+184delinsCAGGGTGGATCGTCCGGGGTGGA...
XM_011518877.3:c.1472+156_1472+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_011517179.1:n.1472+156_1472+184delinsCAGGGTGGATCGTCCGGGGTG...
XM_011518878.3:c.1481+156_1481+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_011517180.1:n.1481+156_1481+184delinsCAGGGTGGATCGTCCGGGGTG...
XM_011518879.3:c.1472+156_1472+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_011517181.1:n.1472+156_1472+184delinsCAGGGTGGATCGTCCGGGGTG...
XM_011518881.3:c.827+156_827+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_011517183.1:n.827+156_827+184delinsCAGGGTGGATCGTCCGGGGTGGA...
XM_017014931.1:c.1271+156_1271+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_016870420.1:n.1271+156_1271+184delinsCAGGGTGGATCGTCCGGGGTG...
XM_017014932.1:c.1094+156_1094+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_016870421.1:n.1094+156_1094+184delinsCAGGGTGGATCGTCCGGGGTG...
XM_017014933.1:c.827+156_827+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_016870422.1:n.827+156_827+184delinsCAGGGTGGATCGTCCGGGGTGGA...
XM_024447617.1:c.827+156_827+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_024303385.1:n.827+156_827+184delinsCAGGGTGGATCGTCCGGGGTGGA...
XM_024447618.1:c.827+156_827+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	XP_024303386.1:n.827+156_827+184delinsCAGGGTGGATCGTCCGGGGTGGA...
NM_020822.3:c.1337+156_1337+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT MANE Select	NP_065873.2:n.1337+156_1337+184delinsCAGGGTGGATCGTCCGGGGTGGAC...
NM_001272003.2:c.1202+156_1202+184delinsCAGGGTGGATCGTCCGGGGTGGACCATTT	NP_001258932.1:n.1202+156_1202+184delinsCAGGGTGGATCGTCCGGGGTG...