Canonical Allele Identifier: CA1883873458

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770374A= , CM000671.2:g.135770374A=	GRCh38
NC_000009.11:g.138662220A= , CM000671.1:g.138662220A=	GRCh37
NC_000009.10:g.137802041A=	NCBI36
NG_033070.1:g.73190A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1696A= MANE Select	ENSP00000360822.2:p.Met566=
ENST00000674572.1:c.1537A=	ENSP00000501742.1:p.Met513=
ENST00000675090.1:c.1444A=	ENSP00000501833.1:p.Met482=
ENST00000675399.1:c.1444A=	ENSP00000501932.1:p.Met482=
ENST00000676421.1:c.1453A=	ENSP00000502322.1:p.Met485=
ENST00000263604.5:c.1597A=	ENSP00000263604.4:p.Met533=
ENST00000371757.6:c.1696A=	ENSP00000360822.2:p.Met566=
ENST00000460750.5:c.*1306A=	ENSP00000418777.1:n.*1306A=
ENST00000486577.6:c.1579A=	ENSP00000417578.3:p.Met527=
ENST00000487664.5:c.1696A=	ENSP00000417851.2:p.Met566=
ENST00000488444.6:c.1639A=	ENSP00000419007.3:p.Met547=
ENST00000490355.6:c.1639A=	ENSP00000418003.3:p.Met547=
ENST00000490363.3:n.1515A=
ENST00000491806.6:c.1639A=	ENSP00000419086.3:p.Met547=
ENST00000628528.2:c.1561A=	ENSP00000486374.1:p.Met521=
ENST00000630792.2:c.1537A=	ENSP00000486486.1:p.Met513=
ENST00000631073.2:c.1639A=	ENSP00000486130.1:p.Met547=
NM_001272003.1:c.1561A=	NP_001258932.1:p.Met521=
NM_020822.2:c.1696A=	NP_065873.2:p.Met566=
XM_011518877.1:c.1831A=	XP_011517179.1:p.Met611=
XM_011518878.1:c.1840A=	XP_011517180.1:p.Met614=
XM_011518879.1:c.1831A=	XP_011517181.1:p.Met611=
XM_011518880.1:c.1597A=	XP_011517182.1:p.Met533=
XM_011518881.1:c.1186A=	XP_011517183.1:p.Met396=
XM_011518877.3:c.1831A=	XP_011517179.1:p.Met611=
XM_011518878.3:c.1840A=	XP_011517180.1:p.Met614=
XM_011518879.3:c.1831A=	XP_011517181.1:p.Met611=
XM_011518881.3:c.1186A=	XP_011517183.1:p.Met396=
XM_017014931.1:c.1630A=	XP_016870420.1:p.Met544=
XM_017014932.1:c.1453A=	XP_016870421.1:p.Met485=
XM_017014933.1:c.1186A=	XP_016870422.1:p.Met396=
XM_024447617.1:c.1186A=	XP_024303385.1:p.Met396=
XM_024447618.1:c.1186A=	XP_024303386.1:p.Met396=
NM_020822.3:c.1696A= MANE Select	NP_065873.2:p.Met566=
NM_001272003.2:c.1561A=	NP_001258932.1:p.Met521=