Canonical Allele Identifier: CA1883866316

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765102G= , CM000671.2:g.135765102G=	GRCh38
NC_000009.11:g.138656948G= , CM000671.1:g.138656948G=	GRCh37
NC_000009.10:g.137796769G=	NCBI36
NG_033070.1:g.67918G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1107G= MANE Select	ENSP00000360822.2:p.Gln369=
ENST00000674572.1:c.948G=	ENSP00000501742.1:p.Gln316=
ENST00000675090.1:c.855G=	ENSP00000501833.1:p.Gln285=
ENST00000675399.1:c.855G=	ENSP00000501932.1:p.Gln285=
ENST00000676421.1:c.864G=	ENSP00000502322.1:p.Gln288=
ENST00000263604.5:c.1008G=	ENSP00000263604.4:p.Gln336=
ENST00000371757.6:c.1107G=	ENSP00000360822.2:p.Gln369=
ENST00000460750.5:c.*717G=	ENSP00000418777.1:n.*717G=
ENST00000486577.6:c.990G=	ENSP00000417578.3:p.Gln330=
ENST00000487664.5:c.1107G=	ENSP00000417851.2:p.Gln369=
ENST00000488444.6:c.1050G=	ENSP00000419007.3:p.Gln350=
ENST00000490355.6:c.1050G=	ENSP00000418003.3:p.Gln350=
ENST00000490363.3:n.926G=
ENST00000491806.6:c.1050G=	ENSP00000419086.3:p.Gln350=
ENST00000628528.2:c.972G=	ENSP00000486374.1:p.Gln324=
ENST00000630792.2:c.948G=	ENSP00000486486.1:p.Gln316=
ENST00000631073.2:c.1050G=	ENSP00000486130.1:p.Gln350=
NM_001272003.1:c.972G=	NP_001258932.1:p.Gln324=
NM_020822.2:c.1107G=	NP_065873.2:p.Gln369=
XM_011518877.1:c.1242G=	XP_011517179.1:p.Gln414=
XM_011518878.1:c.1251G=	XP_011517180.1:p.Gln417=
XM_011518879.1:c.1242G=	XP_011517181.1:p.Gln414=
XM_011518880.1:c.1008G=	XP_011517182.1:p.Gln336=
XM_011518881.1:c.597G=	XP_011517183.1:p.Gln199=
XM_011518877.3:c.1242G=	XP_011517179.1:p.Gln414=
XM_011518878.3:c.1251G=	XP_011517180.1:p.Gln417=
XM_011518879.3:c.1242G=	XP_011517181.1:p.Gln414=
XM_011518881.3:c.597G=	XP_011517183.1:p.Gln199=
XM_017014931.1:c.1041G=	XP_016870420.1:p.Gln347=
XM_017014932.1:c.864G=	XP_016870421.1:p.Gln288=
XM_017014933.1:c.597G=	XP_016870422.1:p.Gln199=
XM_024447617.1:c.597G=	XP_024303385.1:p.Gln199=
XM_024447618.1:c.597G=	XP_024303386.1:p.Gln199=
NM_020822.3:c.1107G= MANE Select	NP_065873.2:p.Gln369=
NM_001272003.2:c.972G=	NP_001258932.1:p.Gln324=