Canonical Allele Identifier: CA375512280

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138667209T>A (hg19) ; chr9:g.135775363T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775363T>A , CM000671.2:g.135775363T>A	GRCh38
NC_000009.11:g.138667209T>A , CM000671.1:g.138667209T>A	GRCh37
NC_000009.10:g.137807030T>A	NCBI36
NG_033070.1:g.78179T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2297T>A MANE Select	ENSP00000360822.2:p.Leu766Gln
ENST00000674572.1:c.2138T>A	ENSP00000501742.1:p.Leu713Gln
ENST00000675090.1:c.2045T>A	ENSP00000501833.1:p.Leu682Gln
ENST00000675399.1:c.2045T>A	ENSP00000501932.1:p.Leu682Gln
ENST00000676421.1:c.2054T>A	ENSP00000502322.1:p.Leu685Gln
ENST00000263604.5:c.2198T>A	ENSP00000263604.4:p.Leu733Gln
ENST00000371757.6:c.2297T>A	ENSP00000360822.2:p.Leu766Gln
ENST00000460750.5:c.*1907T>A	ENSP00000418777.1:n.*1907T>A
ENST00000486577.6:c.2180T>A	ENSP00000417578.3:p.Leu727Gln
ENST00000487664.5:c.2297T>A	ENSP00000417851.2:p.Leu766Gln
ENST00000488444.6:c.2240T>A	ENSP00000419007.3:p.Leu747Gln
ENST00000490355.6:c.2234T>A	ENSP00000418003.3:p.Leu745Gln
ENST00000490363.3:n.2116T>A
ENST00000491806.6:c.2240T>A	ENSP00000419086.3:p.Leu747Gln
ENST00000628528.2:c.2162T>A	ENSP00000486374.1:p.Leu721Gln
ENST00000630792.2:c.2132T>A	ENSP00000486486.1:p.Leu711Gln
ENST00000631073.2:c.2240T>A	ENSP00000486130.1:p.Leu747Gln
ENST00000631193.1:c.146T>A	ENSP00000486830.1:p.Leu49Gln
NM_001272003.1:c.2162T>A	NP_001258932.1:p.Leu721Gln
NM_020822.2:c.2297T>A	NP_065873.2:p.Leu766Gln
XM_011518877.1:c.2432T>A	XP_011517179.1:p.Leu811Gln
XM_011518878.1:c.2441T>A	XP_011517180.1:p.Leu814Gln
XM_011518879.1:c.2432T>A	XP_011517181.1:p.Leu811Gln
XM_011518880.1:c.2198T>A	XP_011517182.1:p.Leu733Gln
XM_011518881.1:c.1787T>A	XP_011517183.1:p.Leu596Gln
XM_011518877.3:c.2432T>A	XP_011517179.1:p.Leu811Gln
XM_011518878.3:c.2441T>A	XP_011517180.1:p.Leu814Gln
XM_011518879.3:c.2432T>A	XP_011517181.1:p.Leu811Gln
XM_011518881.3:c.1787T>A	XP_011517183.1:p.Leu596Gln
XM_017014931.1:c.2231T>A	XP_016870420.1:p.Leu744Gln
XM_017014932.1:c.2054T>A	XP_016870421.1:p.Leu685Gln
XM_017014933.1:c.1787T>A	XP_016870422.1:p.Leu596Gln
XM_024447617.1:c.1787T>A	XP_024303385.1:p.Leu596Gln
XM_024447618.1:c.1787T>A	XP_024303386.1:p.Leu596Gln
NM_020822.3:c.2297T>A MANE Select	NP_065873.2:p.Leu766Gln
NM_001272003.2:c.2162T>A	NP_001258932.1:p.Leu721Gln