Canonical Allele Identifier: CA375506036

Gene: KCNT1

Linked Data

• ClinVar Variation Id: 2953486
• ClinVar RCV Id: RCV003810604
• MyVariant Identifiers: chr9:g.138661891T>A (hg19) ; chr9:g.135770045T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770045T>A , CM000671.2:g.135770045T>A	GRCh38
NC_000009.11:g.138661891T>A , CM000671.1:g.138661891T>A	GRCh37
NC_000009.10:g.137801712T>A	NCBI36
NG_033070.1:g.72861T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1609T>A MANE Select	ENSP00000360822.2:p.Ser537Thr
ENST00000674572.1:c.1450T>A	ENSP00000501742.1:p.Ser484Thr
ENST00000675090.1:c.1357T>A	ENSP00000501833.1:p.Ser453Thr
ENST00000675399.1:c.1357T>A	ENSP00000501932.1:p.Ser453Thr
ENST00000676421.1:c.1366T>A	ENSP00000502322.1:p.Ser456Thr
ENST00000263604.5:c.1510T>A	ENSP00000263604.4:p.Ser504Thr
ENST00000371757.6:c.1609T>A	ENSP00000360822.2:p.Ser537Thr
ENST00000460750.5:c.*1219T>A	ENSP00000418777.1:n.*1219T>A
ENST00000486577.6:c.1492T>A	ENSP00000417578.3:p.Ser498Thr
ENST00000487664.5:c.1609T>A	ENSP00000417851.2:p.Ser537Thr
ENST00000488444.6:c.1552T>A	ENSP00000419007.3:p.Ser518Thr
ENST00000490355.6:c.1552T>A	ENSP00000418003.3:p.Ser518Thr
ENST00000490363.3:n.1428T>A
ENST00000491806.6:c.1552T>A	ENSP00000419086.3:p.Ser518Thr
ENST00000628528.2:c.1474T>A	ENSP00000486374.1:p.Ser492Thr
ENST00000630792.2:c.1450T>A	ENSP00000486486.1:p.Ser484Thr
ENST00000631073.2:c.1552T>A	ENSP00000486130.1:p.Ser518Thr
NM_001272003.1:c.1474T>A	NP_001258932.1:p.Ser492Thr
NM_020822.2:c.1609T>A	NP_065873.2:p.Ser537Thr
XM_011518877.1:c.1744T>A	XP_011517179.1:p.Ser582Thr
XM_011518878.1:c.1753T>A	XP_011517180.1:p.Ser585Thr
XM_011518879.1:c.1744T>A	XP_011517181.1:p.Ser582Thr
XM_011518880.1:c.1510T>A	XP_011517182.1:p.Ser504Thr
XM_011518881.1:c.1099T>A	XP_011517183.1:p.Ser367Thr
XM_011518877.3:c.1744T>A	XP_011517179.1:p.Ser582Thr
XM_011518878.3:c.1753T>A	XP_011517180.1:p.Ser585Thr
XM_011518879.3:c.1744T>A	XP_011517181.1:p.Ser582Thr
XM_011518881.3:c.1099T>A	XP_011517183.1:p.Ser367Thr
XM_017014931.1:c.1543T>A	XP_016870420.1:p.Ser515Thr
XM_017014932.1:c.1366T>A	XP_016870421.1:p.Ser456Thr
XM_017014933.1:c.1099T>A	XP_016870422.1:p.Ser367Thr
XM_024447617.1:c.1099T>A	XP_024303385.1:p.Ser367Thr
XM_024447618.1:c.1099T>A	XP_024303386.1:p.Ser367Thr
NM_020822.3:c.1609T>A MANE Select	NP_065873.2:p.Ser537Thr
NM_001272003.2:c.1474T>A	NP_001258932.1:p.Ser492Thr