Canonical Allele Identifier: CA1883843110

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135750081_135750083delinsCCT , CM000671.2:g.135750081_135750083delinsCCT	GRCh38
NC_000009.11:g.138641927_138641929delinsCCT , CM000671.1:g.138641927_138641929delinsCCT	GRCh37
NC_000009.10:g.137781748_137781750delinsCCT	NCBI36
NG_033070.1:g.52897_52899delinsCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000371757.7:c.255-17_255-15delinsCCT MANE Select	ENSP00000360822.2:n.255-17_255-15delinsCCT
ENST00000637018.1:n.60-17_60-15delinsCCT
ENST00000674572.1:c.96-17_96-15delinsCCT	ENSP00000501742.1:n.96-17_96-15delinsCCT
ENST00000675090.1:c.3-17_3-15delinsCCT	ENSP00000501833.1:n.3-17_3-15delinsCCT
ENST00000675399.1:c.3-17_3-15delinsCCT	ENSP00000501932.1:n.3-17_3-15delinsCCT
ENST00000676421.1:c.3-17_3-15delinsCCT	ENSP00000502322.1:n.3-17_3-15delinsCCT
ENST00000263604.5:c.156-17_156-15delinsCCT	ENSP00000263604.4:n.156-17_156-15delinsCCT
ENST00000371757.6:c.255-17_255-15delinsCCT	ENSP00000360822.2:n.255-17_255-15delinsCCT
ENST00000460750.5:c.255-17_255-15delinsCCT	ENSP00000418777.1:n.255-17_255-15delinsCCT
ENST00000473941.5:c.96-17_96-15delinsCCT	ENSP00000420764.1:n.96-17_96-15delinsCCT
ENST00000486577.6:c.138-17_138-15delinsCCT	ENSP00000417578.3:n.138-17_138-15delinsCCT
ENST00000487664.5:c.255-17_255-15delinsCCT	ENSP00000417851.2:n.255-17_255-15delinsCCT
ENST00000488444.6:c.198-17_198-15delinsCCT	ENSP00000419007.3:n.198-17_198-15delinsCCT
ENST00000490355.6:c.198-17_198-15delinsCCT	ENSP00000418003.3:n.198-17_198-15delinsCCT
ENST00000491806.6:c.198-17_198-15delinsCCT	ENSP00000419086.3:n.198-17_198-15delinsCCT
ENST00000628528.2:c.111-17_111-15delinsCCT	ENSP00000486374.1:n.111-17_111-15delinsCCT
ENST00000630792.2:c.96-17_96-15delinsCCT	ENSP00000486486.1:n.96-17_96-15delinsCCT
ENST00000631073.2:c.198-17_198-15delinsCCT	ENSP00000486130.1:n.198-17_198-15delinsCCT
NM_001272003.1:c.111-17_111-15delinsCCT	NP_001258932.1:n.111-17_111-15delinsCCT
NM_020822.2:c.255-17_255-15delinsCCT	NP_065873.2:n.255-17_255-15delinsCCT
XM_011518877.1:c.390-17_390-15delinsCCT	XP_011517179.1:n.390-17_390-15delinsCCT
XM_011518878.1:c.390-17_390-15delinsCCT	XP_011517180.1:n.390-17_390-15delinsCCT
XM_011518879.1:c.390-17_390-15delinsCCT	XP_011517181.1:n.390-17_390-15delinsCCT
XM_011518880.1:c.156-17_156-15delinsCCT	XP_011517182.1:n.156-17_156-15delinsCCT
XM_011518877.3:c.390-17_390-15delinsCCT	XP_011517179.1:n.390-17_390-15delinsCCT
XM_011518878.3:c.390-17_390-15delinsCCT	XP_011517180.1:n.390-17_390-15delinsCCT
XM_011518879.3:c.390-17_390-15delinsCCT	XP_011517181.1:n.390-17_390-15delinsCCT
XM_017014931.1:c.280-17_280-15delinsCCT	XP_016870420.1:n.280-17_280-15delinsCCT
XM_017014932.1:c.3-17_3-15delinsCCT	XP_016870421.1:n.3-17_3-15delinsCCT
XM_017014933.1:c.-165-17_-165-15delinsCCT	XP_016870422.1:n.-165-17_-165-15delinsCCT
XM_024447617.1:c.-265-17_-265-15delinsCCT	XP_024303385.1:n.-265-17_-265-15delinsCCT
XM_024447618.1:c.-265-17_-265-15delinsCCT	XP_024303386.1:n.-265-17_-265-15delinsCCT
NM_020822.3:c.255-17_255-15delinsCCT MANE Select	NP_065873.2:n.255-17_255-15delinsCCT
NM_001272003.2:c.111-17_111-15delinsCCT	NP_001258932.1:n.111-17_111-15delinsCCT