Canonical Allele Identifier: CA375501526

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138657549A>T (hg19) ; chr9:g.135765703A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765703A>T , CM000671.2:g.135765703A>T	GRCh38
NC_000009.11:g.138657549A>T , CM000671.1:g.138657549A>T	GRCh37
NC_000009.10:g.137797370A>T	NCBI36
NG_033070.1:g.68519A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1280A>T MANE Select	ENSP00000360822.2:p.Gln427Leu
ENST00000636995.1:n.7A>T
ENST00000637798.1:n.19A>T
ENST00000674572.1:c.1121A>T	ENSP00000501742.1:p.Gln374Leu
ENST00000675090.1:c.1028A>T	ENSP00000501833.1:p.Gln343Leu
ENST00000675399.1:c.1028A>T	ENSP00000501932.1:p.Gln343Leu
ENST00000676421.1:c.1037A>T	ENSP00000502322.1:p.Gln346Leu
ENST00000263604.5:c.1181A>T	ENSP00000263604.4:p.Gln394Leu
ENST00000371757.6:c.1280A>T	ENSP00000360822.2:p.Gln427Leu
ENST00000460750.5:c.*890A>T	ENSP00000418777.1:n.*890A>T
ENST00000486577.6:c.1163A>T	ENSP00000417578.3:p.Gln388Leu
ENST00000487664.5:c.1280A>T	ENSP00000417851.2:p.Gln427Leu
ENST00000488444.6:c.1223A>T	ENSP00000419007.3:p.Gln408Leu
ENST00000490355.6:c.1223A>T	ENSP00000418003.3:p.Gln408Leu
ENST00000490363.3:n.1099A>T
ENST00000491806.6:c.1223A>T	ENSP00000419086.3:p.Gln408Leu
ENST00000628528.2:c.1145A>T	ENSP00000486374.1:p.Gln382Leu
ENST00000630792.2:c.1121A>T	ENSP00000486486.1:p.Gln374Leu
ENST00000631073.2:c.1223A>T	ENSP00000486130.1:p.Gln408Leu
NM_001272003.1:c.1145A>T	NP_001258932.1:p.Gln382Leu
NM_020822.2:c.1280A>T	NP_065873.2:p.Gln427Leu
XM_011518877.1:c.1415A>T	XP_011517179.1:p.Gln472Leu
XM_011518878.1:c.1424A>T	XP_011517180.1:p.Gln475Leu
XM_011518879.1:c.1415A>T	XP_011517181.1:p.Gln472Leu
XM_011518880.1:c.1181A>T	XP_011517182.1:p.Gln394Leu
XM_011518881.1:c.770A>T	XP_011517183.1:p.Gln257Leu
XM_011518877.3:c.1415A>T	XP_011517179.1:p.Gln472Leu
XM_011518878.3:c.1424A>T	XP_011517180.1:p.Gln475Leu
XM_011518879.3:c.1415A>T	XP_011517181.1:p.Gln472Leu
XM_011518881.3:c.770A>T	XP_011517183.1:p.Gln257Leu
XM_017014931.1:c.1214A>T	XP_016870420.1:p.Gln405Leu
XM_017014932.1:c.1037A>T	XP_016870421.1:p.Gln346Leu
XM_017014933.1:c.770A>T	XP_016870422.1:p.Gln257Leu
XM_024447617.1:c.770A>T	XP_024303385.1:p.Gln257Leu
XM_024447618.1:c.770A>T	XP_024303386.1:p.Gln257Leu
NM_020822.3:c.1280A>T MANE Select	NP_065873.2:p.Gln427Leu
NM_001272003.2:c.1145A>T	NP_001258932.1:p.Gln382Leu