Canonical Allele Identifier: CA1883866631

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765582_135765583delinsAG , CM000671.2:g.135765582_135765583delinsAG	GRCh38
NC_000009.11:g.138657428_138657429delinsAG , CM000671.1:g.138657428_138657429delinsAG	GRCh37
NC_000009.10:g.137797249_137797250delinsAG	NCBI36
NG_033070.1:g.68398_68399delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1201-42_1201-41delinsAG MANE Select	ENSP00000360822.2:n.1201-42_1201-41delinsAG
ENST00000674572.1:c.1042-42_1042-41delinsAG	ENSP00000501742.1:n.1042-42_1042-41delinsAG
ENST00000675090.1:c.949-42_949-41delinsAG	ENSP00000501833.1:n.949-42_949-41delinsAG
ENST00000675399.1:c.949-42_949-41delinsAG	ENSP00000501932.1:n.949-42_949-41delinsAG
ENST00000676421.1:c.958-42_958-41delinsAG	ENSP00000502322.1:n.958-42_958-41delinsAG
ENST00000263604.5:c.1102-42_1102-41delinsAG	ENSP00000263604.4:n.1102-42_1102-41delinsAG
ENST00000371757.6:c.1201-42_1201-41delinsAG	ENSP00000360822.2:n.1201-42_1201-41delinsAG
ENST00000460750.5:c.*811-42_*811-41delinsAG	ENSP00000418777.1:n.*811-42_*811-41delinsAG
ENST00000486577.6:c.1084-42_1084-41delinsAG	ENSP00000417578.3:n.1084-42_1084-41delinsAG
ENST00000487664.5:c.1201-42_1201-41delinsAG	ENSP00000417851.2:n.1201-42_1201-41delinsAG
ENST00000488444.6:c.1144-42_1144-41delinsAG	ENSP00000419007.3:n.1144-42_1144-41delinsAG
ENST00000490355.6:c.1144-42_1144-41delinsAG	ENSP00000418003.3:n.1144-42_1144-41delinsAG
ENST00000490363.3:n.1020-42_1020-41delinsAG
ENST00000491806.6:c.1144-42_1144-41delinsAG	ENSP00000419086.3:n.1144-42_1144-41delinsAG
ENST00000628528.2:c.1066-42_1066-41delinsAG	ENSP00000486374.1:n.1066-42_1066-41delinsAG
ENST00000630792.2:c.1042-42_1042-41delinsAG	ENSP00000486486.1:n.1042-42_1042-41delinsAG
ENST00000631073.2:c.1144-42_1144-41delinsAG	ENSP00000486130.1:n.1144-42_1144-41delinsAG
NM_001272003.1:c.1066-42_1066-41delinsAG	NP_001258932.1:n.1066-42_1066-41delinsAG
NM_020822.2:c.1201-42_1201-41delinsAG	NP_065873.2:n.1201-42_1201-41delinsAG
XM_011518877.1:c.1336-42_1336-41delinsAG	XP_011517179.1:n.1336-42_1336-41delinsAG
XM_011518878.1:c.1345-42_1345-41delinsAG	XP_011517180.1:n.1345-42_1345-41delinsAG
XM_011518879.1:c.1336-42_1336-41delinsAG	XP_011517181.1:n.1336-42_1336-41delinsAG
XM_011518880.1:c.1102-42_1102-41delinsAG	XP_011517182.1:n.1102-42_1102-41delinsAG
XM_011518881.1:c.691-42_691-41delinsAG	XP_011517183.1:n.691-42_691-41delinsAG
XM_011518877.3:c.1336-42_1336-41delinsAG	XP_011517179.1:n.1336-42_1336-41delinsAG
XM_011518878.3:c.1345-42_1345-41delinsAG	XP_011517180.1:n.1345-42_1345-41delinsAG
XM_011518879.3:c.1336-42_1336-41delinsAG	XP_011517181.1:n.1336-42_1336-41delinsAG
XM_011518881.3:c.691-42_691-41delinsAG	XP_011517183.1:n.691-42_691-41delinsAG
XM_017014931.1:c.1135-42_1135-41delinsAG	XP_016870420.1:n.1135-42_1135-41delinsAG
XM_017014932.1:c.958-42_958-41delinsAG	XP_016870421.1:n.958-42_958-41delinsAG
XM_017014933.1:c.691-42_691-41delinsAG	XP_016870422.1:n.691-42_691-41delinsAG
XM_024447617.1:c.691-42_691-41delinsAG	XP_024303385.1:n.691-42_691-41delinsAG
XM_024447618.1:c.691-42_691-41delinsAG	XP_024303386.1:n.691-42_691-41delinsAG
NM_020822.3:c.1201-42_1201-41delinsAG MANE Select	NP_065873.2:n.1201-42_1201-41delinsAG
NM_001272003.2:c.1066-42_1066-41delinsAG	NP_001258932.1:n.1066-42_1066-41delinsAG