Canonical Allele Identifier: CA1883873590

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770420C= , CM000671.2:g.135770420C=	GRCh38
NC_000009.11:g.138662266C= , CM000671.1:g.138662266C=	GRCh37
NC_000009.10:g.137802087C=	NCBI36
NG_033070.1:g.73236C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1742C= MANE Select	ENSP00000360822.2:p.Thr581=
ENST00000674572.1:c.1583C=	ENSP00000501742.1:p.Thr528=
ENST00000675090.1:c.1490C=	ENSP00000501833.1:p.Thr497=
ENST00000675399.1:c.1490C=	ENSP00000501932.1:p.Thr497=
ENST00000676421.1:c.1499C=	ENSP00000502322.1:p.Thr500=
ENST00000263604.5:c.1643C=	ENSP00000263604.4:p.Thr548=
ENST00000371757.6:c.1742C=	ENSP00000360822.2:p.Thr581=
ENST00000460750.5:c.*1352C=	ENSP00000418777.1:n.*1352C=
ENST00000486577.6:c.1625C=	ENSP00000417578.3:p.Thr542=
ENST00000487664.5:c.1742C=	ENSP00000417851.2:p.Thr581=
ENST00000488444.6:c.1685C=	ENSP00000419007.3:p.Thr562=
ENST00000490355.6:c.1685C=	ENSP00000418003.3:p.Thr562=
ENST00000490363.3:n.1561C=
ENST00000491806.6:c.1685C=	ENSP00000419086.3:p.Thr562=
ENST00000628528.2:c.1607C=	ENSP00000486374.1:p.Thr536=
ENST00000630792.2:c.1583C=	ENSP00000486486.1:p.Thr528=
ENST00000631073.2:c.1685C=	ENSP00000486130.1:p.Thr562=
NM_001272003.1:c.1607C=	NP_001258932.1:p.Thr536=
NM_020822.2:c.1742C=	NP_065873.2:p.Thr581=
XM_011518877.1:c.1877C=	XP_011517179.1:p.Thr626=
XM_011518878.1:c.1886C=	XP_011517180.1:p.Thr629=
XM_011518879.1:c.1877C=	XP_011517181.1:p.Thr626=
XM_011518880.1:c.1643C=	XP_011517182.1:p.Thr548=
XM_011518881.1:c.1232C=	XP_011517183.1:p.Thr411=
XM_011518877.3:c.1877C=	XP_011517179.1:p.Thr626=
XM_011518878.3:c.1886C=	XP_011517180.1:p.Thr629=
XM_011518879.3:c.1877C=	XP_011517181.1:p.Thr626=
XM_011518881.3:c.1232C=	XP_011517183.1:p.Thr411=
XM_017014931.1:c.1676C=	XP_016870420.1:p.Thr559=
XM_017014932.1:c.1499C=	XP_016870421.1:p.Thr500=
XM_017014933.1:c.1232C=	XP_016870422.1:p.Thr411=
XM_024447617.1:c.1232C=	XP_024303385.1:p.Thr411=
XM_024447618.1:c.1232C=	XP_024303386.1:p.Thr411=
NM_020822.3:c.1742C= MANE Select	NP_065873.2:p.Thr581=
NM_001272003.2:c.1607C=	NP_001258932.1:p.Thr536=