Canonical Allele Identifier: CA2692516473

Gene: KCNT1

Linked Data

• gnomAD v4: 9-135765496-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765498del , CM000671.2:g.135765498del	GRCh38
NC_000009.11:g.138657344del , CM000671.1:g.138657344del	GRCh37
NC_000009.10:g.137797165del	NCBI36
NG_033070.1:g.68314del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1201-126del MANE Select	ENSP00000360822.2:n.1201-126del
ENST00000674572.1:c.1042-126del	ENSP00000501742.1:n.1042-126del
ENST00000675090.1:c.949-126del	ENSP00000501833.1:n.949-126del
ENST00000675399.1:c.949-126del	ENSP00000501932.1:n.949-126del
ENST00000676421.1:c.958-126del	ENSP00000502322.1:n.958-126del
ENST00000263604.5:c.1102-126del	ENSP00000263604.4:n.1102-126del
ENST00000371757.6:c.1201-126del	ENSP00000360822.2:n.1201-126del
ENST00000460750.5:c.*811-126del	ENSP00000418777.1:n.*811-126del
ENST00000486577.6:c.1084-126del	ENSP00000417578.3:n.1084-126del
ENST00000487664.5:c.1201-126del	ENSP00000417851.2:n.1201-126del
ENST00000488444.6:c.1144-126del	ENSP00000419007.3:n.1144-126del
ENST00000490355.6:c.1144-126del	ENSP00000418003.3:n.1144-126del
ENST00000490363.3:n.1020-126del
ENST00000491806.6:c.1144-126del	ENSP00000419086.3:n.1144-126del
ENST00000628528.2:c.1066-126del	ENSP00000486374.1:n.1066-126del
ENST00000630792.2:c.1042-126del	ENSP00000486486.1:n.1042-126del
ENST00000631073.2:c.1144-126del	ENSP00000486130.1:n.1144-126del
NM_001272003.1:c.1066-126del	NP_001258932.1:n.1066-126del
NM_020822.2:c.1201-126del	NP_065873.2:n.1201-126del
XM_011518877.1:c.1336-126del	XP_011517179.1:n.1336-126del
XM_011518878.1:c.1345-126del	XP_011517180.1:n.1345-126del
XM_011518879.1:c.1336-126del	XP_011517181.1:n.1336-126del
XM_011518880.1:c.1102-126del	XP_011517182.1:n.1102-126del
XM_011518881.1:c.691-126del	XP_011517183.1:n.691-126del
XM_011518877.3:c.1336-126del	XP_011517179.1:n.1336-126del
XM_011518878.3:c.1345-126del	XP_011517180.1:n.1345-126del
XM_011518879.3:c.1336-126del	XP_011517181.1:n.1336-126del
XM_011518881.3:c.691-126del	XP_011517183.1:n.691-126del
XM_017014931.1:c.1135-126del	XP_016870420.1:n.1135-126del
XM_017014932.1:c.958-126del	XP_016870421.1:n.958-126del
XM_017014933.1:c.691-126del	XP_016870422.1:n.691-126del
XM_024447617.1:c.691-126del	XP_024303385.1:n.691-126del
XM_024447618.1:c.691-126del	XP_024303386.1:n.691-126del
NM_020822.3:c.1201-126del MANE Select	NP_065873.2:n.1201-126del
NM_001272003.2:c.1066-126del	NP_001258932.1:n.1066-126del