Canonical Allele Identifier: CA1883866240

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135764959_135764960delinsGC , CM000671.2:g.135764959_135764960delinsGC	GRCh38
NC_000009.11:g.138656805_138656806delinsGC , CM000671.1:g.138656805_138656806delinsGC	GRCh37
NC_000009.10:g.137796626_137796627delinsGC	NCBI36
NG_033070.1:g.67775_67776delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000371757.7:c.1036-72_1036-71delinsGC MANE Select	ENSP00000360822.2:n.1036-72_1036-71delins...
ENST00000674572.1:c.877-72_877-71delinsGC	ENSP00000501742.1:n.877-72_877-71delinsGC...
ENST00000675090.1:c.784-72_784-71delinsGC	ENSP00000501833.1:n.784-72_784-71delinsGC...
ENST00000675399.1:c.784-72_784-71delinsGC	ENSP00000501932.1:n.784-72_784-71delinsGC...
ENST00000676421.1:c.793-72_793-71delinsGC	ENSP00000502322.1:n.793-72_793-71delinsGC...
ENST00000263604.5:c.937-72_937-71delinsGC	ENSP00000263604.4:n.937-72_937-71delinsGC...
ENST00000371757.6:c.1036-72_1036-71delinsGC	ENSP00000360822.2:n.1036-72_1036-71delins...
ENST00000460750.5:c.*646-72_*646-71delinsGC	ENSP00000418777.1:n.*646-72_*646-71delins...
ENST00000486577.6:c.919-72_919-71delinsGC	ENSP00000417578.3:n.919-72_919-71delinsGC...
ENST00000487664.5:c.1036-72_1036-71delinsGC	ENSP00000417851.2:n.1036-72_1036-71delins...
ENST00000488444.6:c.979-72_979-71delinsGC	ENSP00000419007.3:n.979-72_979-71delinsGC...
ENST00000490355.6:c.979-72_979-71delinsGC	ENSP00000418003.3:n.979-72_979-71delinsGC...
ENST00000490363.3:n.855-72_855-71delinsGC
ENST00000491806.6:c.979-72_979-71delinsGC	ENSP00000419086.3:n.979-72_979-71delinsGC...
ENST00000628528.2:c.901-72_901-71delinsGC	ENSP00000486374.1:n.901-72_901-71delinsGC...
ENST00000630792.2:c.877-72_877-71delinsGC	ENSP00000486486.1:n.877-72_877-71delinsGC...
ENST00000631073.2:c.979-72_979-71delinsGC	ENSP00000486130.1:n.979-72_979-71delinsGC...
NM_001272003.1:c.901-72_901-71delinsGC	NP_001258932.1:n.901-72_901-71delinsGC
NM_020822.2:c.1036-72_1036-71delinsGC	NP_065873.2:n.1036-72_1036-71delinsGC
XM_011518877.1:c.1171-72_1171-71delinsGC	XP_011517179.1:n.1171-72_1171-71delinsGC
XM_011518878.1:c.1180-72_1180-71delinsGC	XP_011517180.1:n.1180-72_1180-71delinsGC
XM_011518879.1:c.1171-72_1171-71delinsGC	XP_011517181.1:n.1171-72_1171-71delinsGC
XM_011518880.1:c.937-72_937-71delinsGC	XP_011517182.1:n.937-72_937-71delinsGC
XM_011518881.1:c.526-72_526-71delinsGC	XP_011517183.1:n.526-72_526-71delinsGC
XM_011518877.3:c.1171-72_1171-71delinsGC	XP_011517179.1:n.1171-72_1171-71delinsGC
XM_011518878.3:c.1180-72_1180-71delinsGC	XP_011517180.1:n.1180-72_1180-71delinsGC
XM_011518879.3:c.1171-72_1171-71delinsGC	XP_011517181.1:n.1171-72_1171-71delinsGC
XM_011518881.3:c.526-72_526-71delinsGC	XP_011517183.1:n.526-72_526-71delinsGC
XM_017014931.1:c.970-72_970-71delinsGC	XP_016870420.1:n.970-72_970-71delinsGC
XM_017014932.1:c.793-72_793-71delinsGC	XP_016870421.1:n.793-72_793-71delinsGC
XM_017014933.1:c.526-72_526-71delinsGC	XP_016870422.1:n.526-72_526-71delinsGC
XM_024447617.1:c.526-72_526-71delinsGC	XP_024303385.1:n.526-72_526-71delinsGC
XM_024447618.1:c.526-72_526-71delinsGC	XP_024303386.1:n.526-72_526-71delinsGC
NM_020822.3:c.1036-72_1036-71delinsGC MANE Select	NP_065873.2:n.1036-72_1036-71delinsGC
NM_001272003.2:c.901-72_901-71delinsGC	NP_001258932.1:n.901-72_901-71delinsGC