Canonical Allele Identifier: CA467698564

Gene: KCNT1

Linked Data

• gnomAD v4: 9-135770421-C-A
• MyVariant Identifiers: chr9:g.138662267C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770421C>A , CM000671.2:g.135770421C>A	GRCh38
NC_000009.11:g.138662267C>A , CM000671.1:g.138662267C>A	GRCh37
NC_000009.10:g.137802088C>A	NCBI36
NG_033070.1:g.73237C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1743C>A MANE Select	ENSP00000360822.2:p.Thr581=
ENST00000674572.1:c.1584C>A	ENSP00000501742.1:p.Thr528=
ENST00000675090.1:c.1491C>A	ENSP00000501833.1:p.Thr497=
ENST00000675399.1:c.1491C>A	ENSP00000501932.1:p.Thr497=
ENST00000676421.1:c.1500C>A	ENSP00000502322.1:p.Thr500=
ENST00000263604.5:c.1644C>A	ENSP00000263604.4:p.Thr548=
ENST00000371757.6:c.1743C>A	ENSP00000360822.2:p.Thr581=
ENST00000460750.5:c.*1353C>A	ENSP00000418777.1:n.*1353C>A
ENST00000486577.6:c.1626C>A	ENSP00000417578.3:p.Thr542=
ENST00000487664.5:c.1743C>A	ENSP00000417851.2:p.Thr581=
ENST00000488444.6:c.1686C>A	ENSP00000419007.3:p.Thr562=
ENST00000490355.6:c.1686C>A	ENSP00000418003.3:p.Thr562=
ENST00000490363.3:n.1562C>A
ENST00000491806.6:c.1686C>A	ENSP00000419086.3:p.Thr562=
ENST00000628528.2:c.1608C>A	ENSP00000486374.1:p.Thr536=
ENST00000630792.2:c.1584C>A	ENSP00000486486.1:p.Thr528=
ENST00000631073.2:c.1686C>A	ENSP00000486130.1:p.Thr562=
NM_001272003.1:c.1608C>A	NP_001258932.1:p.Thr536=
NM_020822.2:c.1743C>A	NP_065873.2:p.Thr581=
XM_011518877.1:c.1878C>A	XP_011517179.1:p.Thr626=
XM_011518878.1:c.1887C>A	XP_011517180.1:p.Thr629=
XM_011518879.1:c.1878C>A	XP_011517181.1:p.Thr626=
XM_011518880.1:c.1644C>A	XP_011517182.1:p.Thr548=
XM_011518881.1:c.1233C>A	XP_011517183.1:p.Thr411=
XM_011518877.3:c.1878C>A	XP_011517179.1:p.Thr626=
XM_011518878.3:c.1887C>A	XP_011517180.1:p.Thr629=
XM_011518879.3:c.1878C>A	XP_011517181.1:p.Thr626=
XM_011518881.3:c.1233C>A	XP_011517183.1:p.Thr411=
XM_017014931.1:c.1677C>A	XP_016870420.1:p.Thr559=
XM_017014932.1:c.1500C>A	XP_016870421.1:p.Thr500=
XM_017014933.1:c.1233C>A	XP_016870422.1:p.Thr411=
XM_024447617.1:c.1233C>A	XP_024303385.1:p.Thr411=
XM_024447618.1:c.1233C>A	XP_024303386.1:p.Thr411=
NM_020822.3:c.1743C>A MANE Select	NP_065873.2:p.Thr581=
NM_001272003.2:c.1608C>A	NP_001258932.1:p.Thr536=