Canonical Allele Identifier: CA375512277

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138667208C>G (hg19) ; chr9:g.135775362C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775362C>G , CM000671.2:g.135775362C>G	GRCh38
NC_000009.11:g.138667208C>G , CM000671.1:g.138667208C>G	GRCh37
NC_000009.10:g.137807029C>G	NCBI36
NG_033070.1:g.78178C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2296C>G MANE Select	ENSP00000360822.2:p.Leu766Val
ENST00000674572.1:c.2137C>G	ENSP00000501742.1:p.Leu713Val
ENST00000675090.1:c.2044C>G	ENSP00000501833.1:p.Leu682Val
ENST00000675399.1:c.2044C>G	ENSP00000501932.1:p.Leu682Val
ENST00000676421.1:c.2053C>G	ENSP00000502322.1:p.Leu685Val
ENST00000263604.5:c.2197C>G	ENSP00000263604.4:p.Leu733Val
ENST00000371757.6:c.2296C>G	ENSP00000360822.2:p.Leu766Val
ENST00000460750.5:c.*1906C>G	ENSP00000418777.1:n.*1906C>G
ENST00000486577.6:c.2179C>G	ENSP00000417578.3:p.Leu727Val
ENST00000487664.5:c.2296C>G	ENSP00000417851.2:p.Leu766Val
ENST00000488444.6:c.2239C>G	ENSP00000419007.3:p.Leu747Val
ENST00000490355.6:c.2233C>G	ENSP00000418003.3:p.Leu745Val
ENST00000490363.3:n.2115C>G
ENST00000491806.6:c.2239C>G	ENSP00000419086.3:p.Leu747Val
ENST00000628528.2:c.2161C>G	ENSP00000486374.1:p.Leu721Val
ENST00000630792.2:c.2131C>G	ENSP00000486486.1:p.Leu711Val
ENST00000631073.2:c.2239C>G	ENSP00000486130.1:p.Leu747Val
ENST00000631193.1:c.145C>G	ENSP00000486830.1:p.Leu49Val
NM_001272003.1:c.2161C>G	NP_001258932.1:p.Leu721Val
NM_020822.2:c.2296C>G	NP_065873.2:p.Leu766Val
XM_011518877.1:c.2431C>G	XP_011517179.1:p.Leu811Val
XM_011518878.1:c.2440C>G	XP_011517180.1:p.Leu814Val
XM_011518879.1:c.2431C>G	XP_011517181.1:p.Leu811Val
XM_011518880.1:c.2197C>G	XP_011517182.1:p.Leu733Val
XM_011518881.1:c.1786C>G	XP_011517183.1:p.Leu596Val
XM_011518877.3:c.2431C>G	XP_011517179.1:p.Leu811Val
XM_011518878.3:c.2440C>G	XP_011517180.1:p.Leu814Val
XM_011518879.3:c.2431C>G	XP_011517181.1:p.Leu811Val
XM_011518881.3:c.1786C>G	XP_011517183.1:p.Leu596Val
XM_017014931.1:c.2230C>G	XP_016870420.1:p.Leu744Val
XM_017014932.1:c.2053C>G	XP_016870421.1:p.Leu685Val
XM_017014933.1:c.1786C>G	XP_016870422.1:p.Leu596Val
XM_024447617.1:c.1786C>G	XP_024303385.1:p.Leu596Val
XM_024447618.1:c.1786C>G	XP_024303386.1:p.Leu596Val
NM_020822.3:c.2296C>G MANE Select	NP_065873.2:p.Leu766Val
NM_001272003.2:c.2161C>G	NP_001258932.1:p.Leu721Val