Canonical Allele Identifier: CA375501846

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138657596A>G (hg19) ; chr9:g.135765750A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765750A>G , CM000671.2:g.135765750A>G	GRCh38
NC_000009.11:g.138657596A>G , CM000671.1:g.138657596A>G	GRCh37
NC_000009.10:g.137797417A>G	NCBI36
NG_033070.1:g.68566A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1327A>G MANE Select	ENSP00000360822.2:p.Met443Val
ENST00000636003.1:c.17A>G
ENST00000636995.1:n.54A>G
ENST00000637798.1:n.66A>G
ENST00000674572.1:c.1168A>G	ENSP00000501742.1:p.Met390Val
ENST00000675090.1:c.1075A>G	ENSP00000501833.1:p.Met359Val
ENST00000675399.1:c.1075A>G	ENSP00000501932.1:p.Met359Val
ENST00000676421.1:c.1084A>G	ENSP00000502322.1:p.Met362Val
ENST00000263604.5:c.1228A>G	ENSP00000263604.4:p.Met410Val
ENST00000371757.6:c.1327A>G	ENSP00000360822.2:p.Met443Val
ENST00000460750.5:c.*937A>G	ENSP00000418777.1:n.*937A>G
ENST00000486577.6:c.1210A>G	ENSP00000417578.3:p.Met404Val
ENST00000487664.5:c.1327A>G	ENSP00000417851.2:p.Met443Val
ENST00000488444.6:c.1270A>G	ENSP00000419007.3:p.Met424Val
ENST00000490355.6:c.1270A>G	ENSP00000418003.3:p.Met424Val
ENST00000490363.3:n.1146A>G
ENST00000491806.6:c.1270A>G	ENSP00000419086.3:p.Met424Val
ENST00000628528.2:c.1192A>G	ENSP00000486374.1:p.Met398Val
ENST00000630792.2:c.1168A>G	ENSP00000486486.1:p.Met390Val
ENST00000631073.2:c.1270A>G	ENSP00000486130.1:p.Met424Val
NM_001272003.1:c.1192A>G	NP_001258932.1:p.Met398Val
NM_020822.2:c.1327A>G	NP_065873.2:p.Met443Val
XM_011518877.1:c.1462A>G	XP_011517179.1:p.Met488Val
XM_011518878.1:c.1471A>G	XP_011517180.1:p.Met491Val
XM_011518879.1:c.1462A>G	XP_011517181.1:p.Met488Val
XM_011518880.1:c.1228A>G	XP_011517182.1:p.Met410Val
XM_011518881.1:c.817A>G	XP_011517183.1:p.Met273Val
XM_011518877.3:c.1462A>G	XP_011517179.1:p.Met488Val
XM_011518878.3:c.1471A>G	XP_011517180.1:p.Met491Val
XM_011518879.3:c.1462A>G	XP_011517181.1:p.Met488Val
XM_011518881.3:c.817A>G	XP_011517183.1:p.Met273Val
XM_017014931.1:c.1261A>G	XP_016870420.1:p.Met421Val
XM_017014932.1:c.1084A>G	XP_016870421.1:p.Met362Val
XM_017014933.1:c.817A>G	XP_016870422.1:p.Met273Val
XM_024447617.1:c.817A>G	XP_024303385.1:p.Met273Val
XM_024447618.1:c.817A>G	XP_024303386.1:p.Met273Val
NM_020822.3:c.1327A>G MANE Select	NP_065873.2:p.Met443Val
NM_001272003.2:c.1192A>G	NP_001258932.1:p.Met398Val