Canonical Allele Identifier: CA375506038

Gene: KCNT1

Linked Data

• ClinVar Variation Id: 2948818
• ClinVar RCV Id: RCV003809592
• dbSNP Id: rs1832640435
• gnomAD v3: 9-135770046-C-A
• gnomAD v4: 9-135770046-C-A
• MyVariant Identifiers: chr9:g.138661892C>A (hg19) ; chr9:g.135770046C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770046C>A , CM000671.2:g.135770046C>A	GRCh38
NC_000009.11:g.138661892C>A , CM000671.1:g.138661892C>A	GRCh37
NC_000009.10:g.137801713C>A	NCBI36
NG_033070.1:g.72862C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1610C>A MANE Select	ENSP00000360822.2:p.Ser537Tyr
ENST00000674572.1:c.1451C>A	ENSP00000501742.1:p.Ser484Tyr
ENST00000675090.1:c.1358C>A	ENSP00000501833.1:p.Ser453Tyr
ENST00000675399.1:c.1358C>A	ENSP00000501932.1:p.Ser453Tyr
ENST00000676421.1:c.1367C>A	ENSP00000502322.1:p.Ser456Tyr
ENST00000263604.5:c.1511C>A	ENSP00000263604.4:p.Ser504Tyr
ENST00000371757.6:c.1610C>A	ENSP00000360822.2:p.Ser537Tyr
ENST00000460750.5:c.*1220C>A	ENSP00000418777.1:n.*1220C>A
ENST00000486577.6:c.1493C>A	ENSP00000417578.3:p.Ser498Tyr
ENST00000487664.5:c.1610C>A	ENSP00000417851.2:p.Ser537Tyr
ENST00000488444.6:c.1553C>A	ENSP00000419007.3:p.Ser518Tyr
ENST00000490355.6:c.1553C>A	ENSP00000418003.3:p.Ser518Tyr
ENST00000490363.3:n.1429C>A
ENST00000491806.6:c.1553C>A	ENSP00000419086.3:p.Ser518Tyr
ENST00000628528.2:c.1475C>A	ENSP00000486374.1:p.Ser492Tyr
ENST00000630792.2:c.1451C>A	ENSP00000486486.1:p.Ser484Tyr
ENST00000631073.2:c.1553C>A	ENSP00000486130.1:p.Ser518Tyr
NM_001272003.1:c.1475C>A	NP_001258932.1:p.Ser492Tyr
NM_020822.2:c.1610C>A	NP_065873.2:p.Ser537Tyr
XM_011518877.1:c.1745C>A	XP_011517179.1:p.Ser582Tyr
XM_011518878.1:c.1754C>A	XP_011517180.1:p.Ser585Tyr
XM_011518879.1:c.1745C>A	XP_011517181.1:p.Ser582Tyr
XM_011518880.1:c.1511C>A	XP_011517182.1:p.Ser504Tyr
XM_011518881.1:c.1100C>A	XP_011517183.1:p.Ser367Tyr
XM_011518877.3:c.1745C>A	XP_011517179.1:p.Ser582Tyr
XM_011518878.3:c.1754C>A	XP_011517180.1:p.Ser585Tyr
XM_011518879.3:c.1745C>A	XP_011517181.1:p.Ser582Tyr
XM_011518881.3:c.1100C>A	XP_011517183.1:p.Ser367Tyr
XM_017014931.1:c.1544C>A	XP_016870420.1:p.Ser515Tyr
XM_017014932.1:c.1367C>A	XP_016870421.1:p.Ser456Tyr
XM_017014933.1:c.1100C>A	XP_016870422.1:p.Ser367Tyr
XM_024447617.1:c.1100C>A	XP_024303385.1:p.Ser367Tyr
XM_024447618.1:c.1100C>A	XP_024303386.1:p.Ser367Tyr
NM_020822.3:c.1610C>A MANE Select	NP_065873.2:p.Ser537Tyr
NM_001272003.2:c.1475C>A	NP_001258932.1:p.Ser492Tyr