Canonical Allele Identifier: CA467698408

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138661860C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770014C>T , CM000671.2:g.135770014C>T	GRCh38
NC_000009.11:g.138661860C>T , CM000671.1:g.138661860C>T	GRCh37
NC_000009.10:g.137801681C>T	NCBI36
NG_033070.1:g.72830C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1578C>T MANE Select	ENSP00000360822.2:p.Thr526=
ENST00000674572.1:c.1419C>T	ENSP00000501742.1:p.Thr473=
ENST00000675090.1:c.1326C>T	ENSP00000501833.1:p.Thr442=
ENST00000675399.1:c.1326C>T	ENSP00000501932.1:p.Thr442=
ENST00000676421.1:c.1335C>T	ENSP00000502322.1:p.Thr445=
ENST00000263604.5:c.1479C>T	ENSP00000263604.4:p.Thr493=
ENST00000371757.6:c.1578C>T	ENSP00000360822.2:p.Thr526=
ENST00000460750.5:c.*1188C>T	ENSP00000418777.1:n.*1188C>T
ENST00000486577.6:c.1461C>T	ENSP00000417578.3:p.Thr487=
ENST00000487664.5:c.1578C>T	ENSP00000417851.2:p.Thr526=
ENST00000488444.6:c.1521C>T	ENSP00000419007.3:p.Thr507=
ENST00000490355.6:c.1521C>T	ENSP00000418003.3:p.Thr507=
ENST00000490363.3:n.1397C>T
ENST00000491806.6:c.1521C>T	ENSP00000419086.3:p.Thr507=
ENST00000628528.2:c.1443C>T	ENSP00000486374.1:p.Thr481=
ENST00000630792.2:c.1419C>T	ENSP00000486486.1:p.Thr473=
ENST00000631073.2:c.1521C>T	ENSP00000486130.1:p.Thr507=
NM_001272003.1:c.1443C>T	NP_001258932.1:p.Thr481=
NM_020822.2:c.1578C>T	NP_065873.2:p.Thr526=
XM_011518877.1:c.1713C>T	XP_011517179.1:p.Thr571=
XM_011518878.1:c.1722C>T	XP_011517180.1:p.Thr574=
XM_011518879.1:c.1713C>T	XP_011517181.1:p.Thr571=
XM_011518880.1:c.1479C>T	XP_011517182.1:p.Thr493=
XM_011518881.1:c.1068C>T	XP_011517183.1:p.Thr356=
XM_011518877.3:c.1713C>T	XP_011517179.1:p.Thr571=
XM_011518878.3:c.1722C>T	XP_011517180.1:p.Thr574=
XM_011518879.3:c.1713C>T	XP_011517181.1:p.Thr571=
XM_011518881.3:c.1068C>T	XP_011517183.1:p.Thr356=
XM_017014931.1:c.1512C>T	XP_016870420.1:p.Thr504=
XM_017014932.1:c.1335C>T	XP_016870421.1:p.Thr445=
XM_017014933.1:c.1068C>T	XP_016870422.1:p.Thr356=
XM_024447617.1:c.1068C>T	XP_024303385.1:p.Thr356=
XM_024447618.1:c.1068C>T	XP_024303386.1:p.Thr356=
NM_020822.3:c.1578C>T MANE Select	NP_065873.2:p.Thr526=
NM_001272003.2:c.1443C>T	NP_001258932.1:p.Thr481=