Canonical Allele Identifier: CA467698817

Gene: KCNT1

Linked Data

• dbSNP Id: rs1307405160
• gnomAD v2: 9-138667243-C-T
• gnomAD v4: 9-135775397-C-T
• MyVariant Identifiers: chr9:g.138667243C>T (hg19) ; chr9:g.135775397C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775397C>T , CM000671.2:g.135775397C>T	GRCh38
NC_000009.11:g.138667243C>T , CM000671.1:g.138667243C>T	GRCh37
NC_000009.10:g.137807064C>T	NCBI36
NG_033070.1:g.78213C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2331C>T MANE Select	ENSP00000360822.2:p.Cys777=
ENST00000674572.1:c.2172C>T	ENSP00000501742.1:p.Cys724=
ENST00000675090.1:c.2079C>T	ENSP00000501833.1:p.Cys693=
ENST00000675399.1:c.2079C>T	ENSP00000501932.1:p.Cys693=
ENST00000676421.1:c.2088C>T	ENSP00000502322.1:p.Cys696=
ENST00000263604.5:c.2232C>T	ENSP00000263604.4:p.Cys744=
ENST00000371757.6:c.2331C>T	ENSP00000360822.2:p.Cys777=
ENST00000460750.5:c.*1941C>T	ENSP00000418777.1:n.*1941C>T
ENST00000486577.6:c.2214C>T	ENSP00000417578.3:p.Cys738=
ENST00000487664.5:c.2331C>T	ENSP00000417851.2:p.Cys777=
ENST00000488444.6:c.2274C>T	ENSP00000419007.3:p.Cys758=
ENST00000490355.6:c.2268C>T	ENSP00000418003.3:p.Cys756=
ENST00000490363.3:n.2150C>T
ENST00000491806.6:c.2274C>T	ENSP00000419086.3:p.Cys758=
ENST00000628528.2:c.2196C>T	ENSP00000486374.1:p.Cys732=
ENST00000630792.2:c.2166C>T	ENSP00000486486.1:p.Cys722=
ENST00000631073.2:c.2274C>T	ENSP00000486130.1:p.Cys758=
ENST00000631193.1:c.180C>T	ENSP00000486830.1:p.Cys60=
NM_001272003.1:c.2196C>T	NP_001258932.1:p.Cys732=
NM_020822.2:c.2331C>T	NP_065873.2:p.Cys777=
XM_011518877.1:c.2466C>T	XP_011517179.1:p.Cys822=
XM_011518878.1:c.2475C>T	XP_011517180.1:p.Cys825=
XM_011518879.1:c.2466C>T	XP_011517181.1:p.Cys822=
XM_011518880.1:c.2232C>T	XP_011517182.1:p.Cys744=
XM_011518881.1:c.1821C>T	XP_011517183.1:p.Cys607=
XM_011518877.3:c.2466C>T	XP_011517179.1:p.Cys822=
XM_011518878.3:c.2475C>T	XP_011517180.1:p.Cys825=
XM_011518879.3:c.2466C>T	XP_011517181.1:p.Cys822=
XM_011518881.3:c.1821C>T	XP_011517183.1:p.Cys607=
XM_017014931.1:c.2265C>T	XP_016870420.1:p.Cys755=
XM_017014932.1:c.2088C>T	XP_016870421.1:p.Cys696=
XM_017014933.1:c.1821C>T	XP_016870422.1:p.Cys607=
XM_024447617.1:c.1821C>T	XP_024303385.1:p.Cys607=
XM_024447618.1:c.1821C>T	XP_024303386.1:p.Cys607=
NM_020822.3:c.2331C>T MANE Select	NP_065873.2:p.Cys777=
NM_001272003.2:c.2196C>T	NP_001258932.1:p.Cys732=