Canonical Allele Identifier: CA375512242

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138667197G>C (hg19) ; chr9:g.135775351G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775351G>C , CM000671.2:g.135775351G>C	GRCh38
NC_000009.11:g.138667197G>C , CM000671.1:g.138667197G>C	GRCh37
NC_000009.10:g.137807018G>C	NCBI36
NG_033070.1:g.78167G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371757.7:c.2285G>C MANE Select	ENSP00000360822.2:p.Ser762Thr
ENST00000674572.1:c.2126G>C	ENSP00000501742.1:p.Ser709Thr
ENST00000675090.1:c.2033G>C	ENSP00000501833.1:p.Ser678Thr
ENST00000675399.1:c.2033G>C	ENSP00000501932.1:p.Ser678Thr
ENST00000676421.1:c.2042G>C	ENSP00000502322.1:p.Ser681Thr
ENST00000263604.5:c.2186G>C	ENSP00000263604.4:p.Ser729Thr
ENST00000371757.6:c.2285G>C	ENSP00000360822.2:p.Ser762Thr
ENST00000460750.5:c.*1895G>C	ENSP00000418777.1:n.*1895G>C
ENST00000486577.6:c.2168G>C	ENSP00000417578.3:p.Ser723Thr
ENST00000487664.5:c.2285G>C	ENSP00000417851.2:p.Ser762Thr
ENST00000488444.6:c.2228G>C	ENSP00000419007.3:p.Ser743Thr
ENST00000490355.6:c.2222G>C	ENSP00000418003.3:p.Ser741Thr
ENST00000490363.3:n.2104G>C
ENST00000491806.6:c.2228G>C	ENSP00000419086.3:p.Ser743Thr
ENST00000628528.2:c.2150G>C	ENSP00000486374.1:p.Ser717Thr
ENST00000630792.2:c.2120G>C	ENSP00000486486.1:p.Ser707Thr
ENST00000631073.2:c.2228G>C	ENSP00000486130.1:p.Ser743Thr
ENST00000631193.1:c.134G>C	ENSP00000486830.1:p.Ser45Thr
NM_001272003.1:c.2150G>C	NP_001258932.1:p.Ser717Thr
NM_020822.2:c.2285G>C	NP_065873.2:p.Ser762Thr
XM_011518877.1:c.2420G>C	XP_011517179.1:p.Ser807Thr
XM_011518878.1:c.2429G>C	XP_011517180.1:p.Ser810Thr
XM_011518879.1:c.2420G>C	XP_011517181.1:p.Ser807Thr
XM_011518880.1:c.2186G>C	XP_011517182.1:p.Ser729Thr
XM_011518881.1:c.1775G>C	XP_011517183.1:p.Ser592Thr
XM_011518877.3:c.2420G>C	XP_011517179.1:p.Ser807Thr
XM_011518878.3:c.2429G>C	XP_011517180.1:p.Ser810Thr
XM_011518879.3:c.2420G>C	XP_011517181.1:p.Ser807Thr
XM_011518881.3:c.1775G>C	XP_011517183.1:p.Ser592Thr
XM_017014931.1:c.2219G>C	XP_016870420.1:p.Ser740Thr
XM_017014932.1:c.2042G>C	XP_016870421.1:p.Ser681Thr
XM_017014933.1:c.1775G>C	XP_016870422.1:p.Ser592Thr
XM_024447617.1:c.1775G>C	XP_024303385.1:p.Ser592Thr
XM_024447618.1:c.1775G>C	XP_024303386.1:p.Ser592Thr
NM_020822.3:c.2285G>C MANE Select	NP_065873.2:p.Ser762Thr
NM_001272003.2:c.2150G>C	NP_001258932.1:p.Ser717Thr