Canonical Allele Identifier: CA375501194

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138657498C>A (hg19) ; chr9:g.135765652C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765652C>A , CM000671.2:g.135765652C>A	GRCh38
NC_000009.11:g.138657498C>A , CM000671.1:g.138657498C>A	GRCh37
NC_000009.10:g.137797319C>A	NCBI36
NG_033070.1:g.68468C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1229C>A MANE Select	ENSP00000360822.2:p.Thr410Lys
ENST00000674572.1:c.1070C>A	ENSP00000501742.1:p.Thr357Lys
ENST00000675090.1:c.977C>A	ENSP00000501833.1:p.Thr326Lys
ENST00000675399.1:c.977C>A	ENSP00000501932.1:p.Thr326Lys
ENST00000676421.1:c.986C>A	ENSP00000502322.1:p.Thr329Lys
ENST00000263604.5:c.1130C>A	ENSP00000263604.4:p.Thr377Lys
ENST00000371757.6:c.1229C>A	ENSP00000360822.2:p.Thr410Lys
ENST00000460750.5:c.*839C>A	ENSP00000418777.1:n.*839C>A
ENST00000486577.6:c.1112C>A	ENSP00000417578.3:p.Thr371Lys
ENST00000487664.5:c.1229C>A	ENSP00000417851.2:p.Thr410Lys
ENST00000488444.6:c.1172C>A	ENSP00000419007.3:p.Thr391Lys
ENST00000490355.6:c.1172C>A	ENSP00000418003.3:p.Thr391Lys
ENST00000490363.3:n.1048C>A
ENST00000491806.6:c.1172C>A	ENSP00000419086.3:p.Thr391Lys
ENST00000628528.2:c.1094C>A	ENSP00000486374.1:p.Thr365Lys
ENST00000630792.2:c.1070C>A	ENSP00000486486.1:p.Thr357Lys
ENST00000631073.2:c.1172C>A	ENSP00000486130.1:p.Thr391Lys
NM_001272003.1:c.1094C>A	NP_001258932.1:p.Thr365Lys
NM_020822.2:c.1229C>A	NP_065873.2:p.Thr410Lys
XM_011518877.1:c.1364C>A	XP_011517179.1:p.Thr455Lys
XM_011518878.1:c.1373C>A	XP_011517180.1:p.Thr458Lys
XM_011518879.1:c.1364C>A	XP_011517181.1:p.Thr455Lys
XM_011518880.1:c.1130C>A	XP_011517182.1:p.Thr377Lys
XM_011518881.1:c.719C>A	XP_011517183.1:p.Thr240Lys
XM_011518877.3:c.1364C>A	XP_011517179.1:p.Thr455Lys
XM_011518878.3:c.1373C>A	XP_011517180.1:p.Thr458Lys
XM_011518879.3:c.1364C>A	XP_011517181.1:p.Thr455Lys
XM_011518881.3:c.719C>A	XP_011517183.1:p.Thr240Lys
XM_017014931.1:c.1163C>A	XP_016870420.1:p.Thr388Lys
XM_017014932.1:c.986C>A	XP_016870421.1:p.Thr329Lys
XM_017014933.1:c.719C>A	XP_016870422.1:p.Thr240Lys
XM_024447617.1:c.719C>A	XP_024303385.1:p.Thr240Lys
XM_024447618.1:c.719C>A	XP_024303386.1:p.Thr240Lys
NM_020822.3:c.1229C>A MANE Select	NP_065873.2:p.Thr410Lys
NM_001272003.2:c.1094C>A	NP_001258932.1:p.Thr365Lys