Canonical Allele Identifier: CA1883843198

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135750102C= , CM000671.2:g.135750102C=	GRCh38
NC_000009.11:g.138641948C= , CM000671.1:g.138641948C=	GRCh37
NC_000009.10:g.137781769C=	NCBI36
NG_033070.1:g.52918C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.259C= MANE Select	ENSP00000360822.2:p.Gln87=
ENST00000637018.1:n.64C=
ENST00000674572.1:c.100C=	ENSP00000501742.1:p.Gln34=
ENST00000675090.1:c.7C=	ENSP00000501833.1:p.Gln3=
ENST00000675399.1:c.7C=	ENSP00000501932.1:p.Gln3=
ENST00000676421.1:c.7C=	ENSP00000502322.1:p.Gln3=
ENST00000263604.5:c.160C=	ENSP00000263604.4:p.Gln54=
ENST00000371757.6:c.259C=	ENSP00000360822.2:p.Gln87=
ENST00000460750.5:c.259C=	ENSP00000418777.1:p.Gln87=
ENST00000473941.5:c.100C=	ENSP00000420764.1:p.Gln34=
ENST00000486577.6:c.142C=	ENSP00000417578.3:p.Gln48=
ENST00000487664.5:c.259C=	ENSP00000417851.2:p.Gln87=
ENST00000488444.6:c.202C=	ENSP00000419007.3:p.Gln68=
ENST00000490355.6:c.202C=	ENSP00000418003.3:p.Gln68=
ENST00000491806.6:c.202C=	ENSP00000419086.3:p.Gln68=
ENST00000628528.2:c.115C=	ENSP00000486374.1:p.Gln39=
ENST00000630792.2:c.100C=	ENSP00000486486.1:p.Gln34=
ENST00000631073.2:c.202C=	ENSP00000486130.1:p.Gln68=
NM_001272003.1:c.115C=	NP_001258932.1:p.Gln39=
NM_020822.2:c.259C=	NP_065873.2:p.Gln87=
XM_011518877.1:c.394C=	XP_011517179.1:p.Gln132=
XM_011518878.1:c.394C=	XP_011517180.1:p.Gln132=
XM_011518879.1:c.394C=	XP_011517181.1:p.Gln132=
XM_011518880.1:c.160C=	XP_011517182.1:p.Gln54=
XM_011518877.3:c.394C=	XP_011517179.1:p.Gln132=
XM_011518878.3:c.394C=	XP_011517180.1:p.Gln132=
XM_011518879.3:c.394C=	XP_011517181.1:p.Gln132=
XM_017014931.1:c.284C=	XP_016870420.1:p.Pro95=
XM_017014932.1:c.7C=	XP_016870421.1:p.Gln3=
XM_017014933.1:c.-161C=	XP_016870422.1:n.-161C=
XM_024447617.1:c.-261C=	XP_024303385.1:n.-261C=
XM_024447618.1:c.-261C=	XP_024303386.1:n.-261C=
NM_020822.3:c.259C= MANE Select	NP_065873.2:p.Gln87=
NM_001272003.2:c.115C=	NP_001258932.1:p.Gln39=