Canonical Allele Identifier: CA375512292

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138667211T>A (hg19) ; chr9:g.135775365T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775365T>A , CM000671.2:g.135775365T>A	GRCh38
NC_000009.11:g.138667211T>A , CM000671.1:g.138667211T>A	GRCh37
NC_000009.10:g.137807032T>A	NCBI36
NG_033070.1:g.78181T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2299T>A MANE Select	ENSP00000360822.2:p.Cys767Ser
ENST00000674572.1:c.2140T>A	ENSP00000501742.1:p.Cys714Ser
ENST00000675090.1:c.2047T>A	ENSP00000501833.1:p.Cys683Ser
ENST00000675399.1:c.2047T>A	ENSP00000501932.1:p.Cys683Ser
ENST00000676421.1:c.2056T>A	ENSP00000502322.1:p.Cys686Ser
ENST00000263604.5:c.2200T>A	ENSP00000263604.4:p.Cys734Ser
ENST00000371757.6:c.2299T>A	ENSP00000360822.2:p.Cys767Ser
ENST00000460750.5:c.*1909T>A	ENSP00000418777.1:n.*1909T>A
ENST00000486577.6:c.2182T>A	ENSP00000417578.3:p.Cys728Ser
ENST00000487664.5:c.2299T>A	ENSP00000417851.2:p.Cys767Ser
ENST00000488444.6:c.2242T>A	ENSP00000419007.3:p.Cys748Ser
ENST00000490355.6:c.2236T>A	ENSP00000418003.3:p.Cys746Ser
ENST00000490363.3:n.2118T>A
ENST00000491806.6:c.2242T>A	ENSP00000419086.3:p.Cys748Ser
ENST00000628528.2:c.2164T>A	ENSP00000486374.1:p.Cys722Ser
ENST00000630792.2:c.2134T>A	ENSP00000486486.1:p.Cys712Ser
ENST00000631073.2:c.2242T>A	ENSP00000486130.1:p.Cys748Ser
ENST00000631193.1:c.148T>A	ENSP00000486830.1:p.Cys50Ser
NM_001272003.1:c.2164T>A	NP_001258932.1:p.Cys722Ser
NM_020822.2:c.2299T>A	NP_065873.2:p.Cys767Ser
XM_011518877.1:c.2434T>A	XP_011517179.1:p.Cys812Ser
XM_011518878.1:c.2443T>A	XP_011517180.1:p.Cys815Ser
XM_011518879.1:c.2434T>A	XP_011517181.1:p.Cys812Ser
XM_011518880.1:c.2200T>A	XP_011517182.1:p.Cys734Ser
XM_011518881.1:c.1789T>A	XP_011517183.1:p.Cys597Ser
XM_011518877.3:c.2434T>A	XP_011517179.1:p.Cys812Ser
XM_011518878.3:c.2443T>A	XP_011517180.1:p.Cys815Ser
XM_011518879.3:c.2434T>A	XP_011517181.1:p.Cys812Ser
XM_011518881.3:c.1789T>A	XP_011517183.1:p.Cys597Ser
XM_017014931.1:c.2233T>A	XP_016870420.1:p.Cys745Ser
XM_017014932.1:c.2056T>A	XP_016870421.1:p.Cys686Ser
XM_017014933.1:c.1789T>A	XP_016870422.1:p.Cys597Ser
XM_024447617.1:c.1789T>A	XP_024303385.1:p.Cys597Ser
XM_024447618.1:c.1789T>A	XP_024303386.1:p.Cys597Ser
NM_020822.3:c.2299T>A MANE Select	NP_065873.2:p.Cys767Ser
NM_001272003.2:c.2164T>A	NP_001258932.1:p.Cys722Ser