Canonical Allele Identifier: CA375505905

Gene: KCNT1

Linked Data

• gnomAD v4: 9-135769980-C-T
• MyVariant Identifiers: chr9:g.138661826C>T (hg19) ; chr9:g.135769980C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135769980C>T , CM000671.2:g.135769980C>T	GRCh38
NC_000009.11:g.138661826C>T , CM000671.1:g.138661826C>T	GRCh37
NC_000009.10:g.137801647C>T	NCBI36
NG_033070.1:g.72796C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1544C>T MANE Select	ENSP00000360822.2:p.Ala515Val
ENST00000674572.1:c.1385C>T	ENSP00000501742.1:p.Ala462Val
ENST00000675090.1:c.1292C>T	ENSP00000501833.1:p.Ala431Val
ENST00000675399.1:c.1292C>T	ENSP00000501932.1:p.Ala431Val
ENST00000676421.1:c.1301C>T	ENSP00000502322.1:p.Ala434Val
ENST00000263604.5:c.1445C>T	ENSP00000263604.4:p.Ala482Val
ENST00000371757.6:c.1544C>T	ENSP00000360822.2:p.Ala515Val
ENST00000460750.5:c.*1154C>T	ENSP00000418777.1:n.*1154C>T
ENST00000486577.6:c.1427C>T	ENSP00000417578.3:p.Ala476Val
ENST00000487664.5:c.1544C>T	ENSP00000417851.2:p.Ala515Val
ENST00000488444.6:c.1487C>T	ENSP00000419007.3:p.Ala496Val
ENST00000490355.6:c.1487C>T	ENSP00000418003.3:p.Ala496Val
ENST00000490363.3:n.1363C>T
ENST00000491806.6:c.1487C>T	ENSP00000419086.3:p.Ala496Val
ENST00000628528.2:c.1409C>T	ENSP00000486374.1:p.Ala470Val
ENST00000630792.2:c.1385C>T	ENSP00000486486.1:p.Ala462Val
ENST00000631073.2:c.1487C>T	ENSP00000486130.1:p.Ala496Val
NM_001272003.1:c.1409C>T	NP_001258932.1:p.Ala470Val
NM_020822.2:c.1544C>T	NP_065873.2:p.Ala515Val
XM_011518877.1:c.1679C>T	XP_011517179.1:p.Ala560Val
XM_011518878.1:c.1688C>T	XP_011517180.1:p.Ala563Val
XM_011518879.1:c.1679C>T	XP_011517181.1:p.Ala560Val
XM_011518880.1:c.1445C>T	XP_011517182.1:p.Ala482Val
XM_011518881.1:c.1034C>T	XP_011517183.1:p.Ala345Val
XM_011518877.3:c.1679C>T	XP_011517179.1:p.Ala560Val
XM_011518878.3:c.1688C>T	XP_011517180.1:p.Ala563Val
XM_011518879.3:c.1679C>T	XP_011517181.1:p.Ala560Val
XM_011518881.3:c.1034C>T	XP_011517183.1:p.Ala345Val
XM_017014931.1:c.1478C>T	XP_016870420.1:p.Ala493Val
XM_017014932.1:c.1301C>T	XP_016870421.1:p.Ala434Val
XM_017014933.1:c.1034C>T	XP_016870422.1:p.Ala345Val
XM_024447617.1:c.1034C>T	XP_024303385.1:p.Ala345Val
XM_024447618.1:c.1034C>T	XP_024303386.1:p.Ala345Val
NM_020822.3:c.1544C>T MANE Select	NP_065873.2:p.Ala515Val
NM_001272003.2:c.1409C>T	NP_001258932.1:p.Ala470Val