Canonical Allele Identifier: CA375506773

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138662264C>G (hg19) ; chr9:g.135770418C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770418C>G , CM000671.2:g.135770418C>G	GRCh38
NC_000009.11:g.138662264C>G , CM000671.1:g.138662264C>G	GRCh37
NC_000009.10:g.137802085C>G	NCBI36
NG_033070.1:g.73234C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1740C>G MANE Select	ENSP00000360822.2:p.Phe580Leu
ENST00000674572.1:c.1581C>G	ENSP00000501742.1:p.Phe527Leu
ENST00000675090.1:c.1488C>G	ENSP00000501833.1:p.Phe496Leu
ENST00000675399.1:c.1488C>G	ENSP00000501932.1:p.Phe496Leu
ENST00000676421.1:c.1497C>G	ENSP00000502322.1:p.Phe499Leu
ENST00000263604.5:c.1641C>G	ENSP00000263604.4:p.Phe547Leu
ENST00000371757.6:c.1740C>G	ENSP00000360822.2:p.Phe580Leu
ENST00000460750.5:c.*1350C>G	ENSP00000418777.1:n.*1350C>G
ENST00000486577.6:c.1623C>G	ENSP00000417578.3:p.Phe541Leu
ENST00000487664.5:c.1740C>G	ENSP00000417851.2:p.Phe580Leu
ENST00000488444.6:c.1683C>G	ENSP00000419007.3:p.Phe561Leu
ENST00000490355.6:c.1683C>G	ENSP00000418003.3:p.Phe561Leu
ENST00000490363.3:n.1559C>G
ENST00000491806.6:c.1683C>G	ENSP00000419086.3:p.Phe561Leu
ENST00000628528.2:c.1605C>G	ENSP00000486374.1:p.Phe535Leu
ENST00000630792.2:c.1581C>G	ENSP00000486486.1:p.Phe527Leu
ENST00000631073.2:c.1683C>G	ENSP00000486130.1:p.Phe561Leu
NM_001272003.1:c.1605C>G	NP_001258932.1:p.Phe535Leu
NM_020822.2:c.1740C>G	NP_065873.2:p.Phe580Leu
XM_011518877.1:c.1875C>G	XP_011517179.1:p.Phe625Leu
XM_011518878.1:c.1884C>G	XP_011517180.1:p.Phe628Leu
XM_011518879.1:c.1875C>G	XP_011517181.1:p.Phe625Leu
XM_011518880.1:c.1641C>G	XP_011517182.1:p.Phe547Leu
XM_011518881.1:c.1230C>G	XP_011517183.1:p.Phe410Leu
XM_011518877.3:c.1875C>G	XP_011517179.1:p.Phe625Leu
XM_011518878.3:c.1884C>G	XP_011517180.1:p.Phe628Leu
XM_011518879.3:c.1875C>G	XP_011517181.1:p.Phe625Leu
XM_011518881.3:c.1230C>G	XP_011517183.1:p.Phe410Leu
XM_017014931.1:c.1674C>G	XP_016870420.1:p.Phe558Leu
XM_017014932.1:c.1497C>G	XP_016870421.1:p.Phe499Leu
XM_017014933.1:c.1230C>G	XP_016870422.1:p.Phe410Leu
XM_024447617.1:c.1230C>G	XP_024303385.1:p.Phe410Leu
XM_024447618.1:c.1230C>G	XP_024303386.1:p.Phe410Leu
NM_020822.3:c.1740C>G MANE Select	NP_065873.2:p.Phe580Leu
NM_001272003.2:c.1605C>G	NP_001258932.1:p.Phe535Leu