Canonical Allele Identifier: CA201476133

Gene: KCNT1

Linked Data

• dbSNP Id: rs907261817
• gnomAD v3: 9-135775349-C-T
• gnomAD v4: 9-135775349-C-T
• MyVariant Identifiers: chr9:g.138667195C>T (hg19) ; chr9:g.135775349C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775349C>T , CM000671.2:g.135775349C>T	GRCh38
NC_000009.11:g.138667195C>T , CM000671.1:g.138667195C>T	GRCh37
NC_000009.10:g.137807016C>T	NCBI36
NG_033070.1:g.78165C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371757.7:c.2283C>T MANE Select	ENSP00000360822.2:p.Gly761=
ENST00000674572.1:c.2124C>T	ENSP00000501742.1:p.Gly708=
ENST00000675090.1:c.2031C>T	ENSP00000501833.1:p.Gly677=
ENST00000675399.1:c.2031C>T	ENSP00000501932.1:p.Gly677=
ENST00000676421.1:c.2040C>T	ENSP00000502322.1:p.Gly680=
ENST00000263604.5:c.2184C>T	ENSP00000263604.4:p.Gly728=
ENST00000371757.6:c.2283C>T	ENSP00000360822.2:p.Gly761=
ENST00000460750.5:c.*1893C>T	ENSP00000418777.1:n.*1893C>T
ENST00000486577.6:c.2166C>T	ENSP00000417578.3:p.Gly722=
ENST00000487664.5:c.2283C>T	ENSP00000417851.2:p.Gly761=
ENST00000488444.6:c.2226C>T	ENSP00000419007.3:p.Gly742=
ENST00000490355.6:c.2220C>T	ENSP00000418003.3:p.Gly740=
ENST00000490363.3:n.2102C>T
ENST00000491806.6:c.2226C>T	ENSP00000419086.3:p.Gly742=
ENST00000628528.2:c.2148C>T	ENSP00000486374.1:p.Gly716=
ENST00000630792.2:c.2118C>T	ENSP00000486486.1:p.Gly706=
ENST00000631073.2:c.2226C>T	ENSP00000486130.1:p.Gly742=
ENST00000631193.1:c.132C>T	ENSP00000486830.1:p.Gly44=
NM_001272003.1:c.2148C>T	NP_001258932.1:p.Gly716=
NM_020822.2:c.2283C>T	NP_065873.2:p.Gly761=
XM_011518877.1:c.2418C>T	XP_011517179.1:p.Gly806=
XM_011518878.1:c.2427C>T	XP_011517180.1:p.Gly809=
XM_011518879.1:c.2418C>T	XP_011517181.1:p.Gly806=
XM_011518880.1:c.2184C>T	XP_011517182.1:p.Gly728=
XM_011518881.1:c.1773C>T	XP_011517183.1:p.Gly591=
XM_011518877.3:c.2418C>T	XP_011517179.1:p.Gly806=
XM_011518878.3:c.2427C>T	XP_011517180.1:p.Gly809=
XM_011518879.3:c.2418C>T	XP_011517181.1:p.Gly806=
XM_011518881.3:c.1773C>T	XP_011517183.1:p.Gly591=
XM_017014931.1:c.2217C>T	XP_016870420.1:p.Gly739=
XM_017014932.1:c.2040C>T	XP_016870421.1:p.Gly680=
XM_017014933.1:c.1773C>T	XP_016870422.1:p.Gly591=
XM_024447617.1:c.1773C>T	XP_024303385.1:p.Gly591=
XM_024447618.1:c.1773C>T	XP_024303386.1:p.Gly591=
NM_020822.3:c.2283C>T MANE Select	NP_065873.2:p.Gly761=
NM_001272003.2:c.2148C>T	NP_001258932.1:p.Gly716=