Canonical Allele Identifier: CA375512196

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138667182C>G (hg19) ; chr9:g.135775336C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775336C>G , CM000671.2:g.135775336C>G	GRCh38
NC_000009.11:g.138667182C>G , CM000671.1:g.138667182C>G	GRCh37
NC_000009.10:g.137807003C>G	NCBI36
NG_033070.1:g.78152C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2270C>G MANE Select	ENSP00000360822.2:p.Ser757Trp
ENST00000674572.1:c.2111C>G	ENSP00000501742.1:p.Ser704Trp
ENST00000675090.1:c.2018C>G	ENSP00000501833.1:p.Ser673Trp
ENST00000675399.1:c.2018C>G	ENSP00000501932.1:p.Ser673Trp
ENST00000676421.1:c.2027C>G	ENSP00000502322.1:p.Ser676Trp
ENST00000263604.5:c.2171C>G	ENSP00000263604.4:p.Ser724Trp
ENST00000371757.6:c.2270C>G	ENSP00000360822.2:p.Ser757Trp
ENST00000460750.5:c.*1880C>G	ENSP00000418777.1:n.*1880C>G
ENST00000486577.6:c.2153C>G	ENSP00000417578.3:p.Ser718Trp
ENST00000487664.5:c.2270C>G	ENSP00000417851.2:p.Ser757Trp
ENST00000488444.6:c.2213C>G	ENSP00000419007.3:p.Ser738Trp
ENST00000490355.6:c.2207C>G	ENSP00000418003.3:p.Ser736Trp
ENST00000490363.3:n.2089C>G
ENST00000491806.6:c.2213C>G	ENSP00000419086.3:p.Ser738Trp
ENST00000628528.2:c.2135C>G	ENSP00000486374.1:p.Ser712Trp
ENST00000630792.2:c.2105C>G	ENSP00000486486.1:p.Ser702Trp
ENST00000631073.2:c.2213C>G	ENSP00000486130.1:p.Ser738Trp
ENST00000631193.1:c.119C>G	ENSP00000486830.1:p.Ser40Trp
NM_001272003.1:c.2135C>G	NP_001258932.1:p.Ser712Trp
NM_020822.2:c.2270C>G	NP_065873.2:p.Ser757Trp
XM_011518877.1:c.2405C>G	XP_011517179.1:p.Ser802Trp
XM_011518878.1:c.2414C>G	XP_011517180.1:p.Ser805Trp
XM_011518879.1:c.2405C>G	XP_011517181.1:p.Ser802Trp
XM_011518880.1:c.2171C>G	XP_011517182.1:p.Ser724Trp
XM_011518881.1:c.1760C>G	XP_011517183.1:p.Ser587Trp
XM_011518877.3:c.2405C>G	XP_011517179.1:p.Ser802Trp
XM_011518878.3:c.2414C>G	XP_011517180.1:p.Ser805Trp
XM_011518879.3:c.2405C>G	XP_011517181.1:p.Ser802Trp
XM_011518881.3:c.1760C>G	XP_011517183.1:p.Ser587Trp
XM_017014931.1:c.2204C>G	XP_016870420.1:p.Ser735Trp
XM_017014932.1:c.2027C>G	XP_016870421.1:p.Ser676Trp
XM_017014933.1:c.1760C>G	XP_016870422.1:p.Ser587Trp
XM_024447617.1:c.1760C>G	XP_024303385.1:p.Ser587Trp
XM_024447618.1:c.1760C>G	XP_024303386.1:p.Ser587Trp
NM_020822.3:c.2270C>G MANE Select	NP_065873.2:p.Ser757Trp
NM_001272003.2:c.2135C>G	NP_001258932.1:p.Ser712Trp