Canonical Allele Identifier: CA1883885034

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775422_135775423delinsCT , CM000671.2:g.135775422_135775423delinsCT	GRCh38
NC_000009.11:g.138667268_138667269delinsCT , CM000671.1:g.138667268_138667269delinsCT	GRCh37
NC_000009.10:g.137807089_137807090delinsCT	NCBI36
NG_033070.1:g.78238_78239delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2349+7_2349+8delinsCT MANE Select	ENSP00000360822.2:n.2349+7_2349+8delinsCT
ENST00000674572.1:c.2190+7_2190+8delinsCT	ENSP00000501742.1:n.2190+7_2190+8delinsCT
ENST00000675090.1:c.2097+7_2097+8delinsCT	ENSP00000501833.1:n.2097+7_2097+8delinsCT
ENST00000675399.1:c.2097+7_2097+8delinsCT	ENSP00000501932.1:n.2097+7_2097+8delinsCT
ENST00000676421.1:c.2106+7_2106+8delinsCT	ENSP00000502322.1:n.2106+7_2106+8delinsCT
ENST00000263604.5:c.2250+7_2250+8delinsCT	ENSP00000263604.4:n.2250+7_2250+8delinsCT
ENST00000371757.6:c.2349+7_2349+8delinsCT	ENSP00000360822.2:n.2349+7_2349+8delinsCT
ENST00000460750.5:c.*1959+7_*1959+8delinsCT	ENSP00000418777.1:n.*1959+7_*1959+8delinsCT
ENST00000486577.6:c.2232+7_2232+8delinsCT	ENSP00000417578.3:n.2232+7_2232+8delinsCT
ENST00000487664.5:c.2349+7_2349+8delinsCT	ENSP00000417851.2:n.2349+7_2349+8delinsCT
ENST00000488444.6:c.2292+7_2292+8delinsCT	ENSP00000419007.3:n.2292+7_2292+8delinsCT
ENST00000490355.6:c.2286+7_2286+8delinsCT	ENSP00000418003.3:n.2286+7_2286+8delinsCT
ENST00000490363.3:n.2168+7_2168+8delinsCT
ENST00000491806.6:c.2292+7_2292+8delinsCT	ENSP00000419086.3:n.2292+7_2292+8delinsCT
ENST00000628528.2:c.2214+7_2214+8delinsCT	ENSP00000486374.1:n.2214+7_2214+8delinsCT
ENST00000630792.2:c.2184+7_2184+8delinsCT	ENSP00000486486.1:n.2184+7_2184+8delinsCT
ENST00000631073.2:c.2292+7_2292+8delinsCT	ENSP00000486130.1:n.2292+7_2292+8delinsCT
ENST00000631193.1:c.198+7_198+8delinsCT	ENSP00000486830.1:n.198+7_198+8delinsCT
NM_001272003.1:c.2214+7_2214+8delinsCT	NP_001258932.1:n.2214+7_2214+8delinsCT
NM_020822.2:c.2349+7_2349+8delinsCT	NP_065873.2:n.2349+7_2349+8delinsCT
XM_011518877.1:c.2484+7_2484+8delinsCT	XP_011517179.1:n.2484+7_2484+8delinsCT
XM_011518878.1:c.2493+7_2493+8delinsCT	XP_011517180.1:n.2493+7_2493+8delinsCT
XM_011518879.1:c.2484+7_2484+8delinsCT	XP_011517181.1:n.2484+7_2484+8delinsCT
XM_011518880.1:c.2250+7_2250+8delinsCT	XP_011517182.1:n.2250+7_2250+8delinsCT
XM_011518881.1:c.1839+7_1839+8delinsCT	XP_011517183.1:n.1839+7_1839+8delinsCT
XM_011518877.3:c.2484+7_2484+8delinsCT	XP_011517179.1:n.2484+7_2484+8delinsCT
XM_011518878.3:c.2493+7_2493+8delinsCT	XP_011517180.1:n.2493+7_2493+8delinsCT
XM_011518879.3:c.2484+7_2484+8delinsCT	XP_011517181.1:n.2484+7_2484+8delinsCT
XM_011518881.3:c.1839+7_1839+8delinsCT	XP_011517183.1:n.1839+7_1839+8delinsCT
XM_017014931.1:c.2283+7_2283+8delinsCT	XP_016870420.1:n.2283+7_2283+8delinsCT
XM_017014932.1:c.2106+7_2106+8delinsCT	XP_016870421.1:n.2106+7_2106+8delinsCT
XM_017014933.1:c.1839+7_1839+8delinsCT	XP_016870422.1:n.1839+7_1839+8delinsCT
XM_024447617.1:c.1839+7_1839+8delinsCT	XP_024303385.1:n.1839+7_1839+8delinsCT
XM_024447618.1:c.1839+7_1839+8delinsCT	XP_024303386.1:n.1839+7_1839+8delinsCT
NM_020822.3:c.2349+7_2349+8delinsCT MANE Select	NP_065873.2:n.2349+7_2349+8delinsCT
NM_001272003.2:c.2214+7_2214+8delinsCT	NP_001258932.1:n.2214+7_2214+8delinsCT