Canonical Allele Identifier: CA375506791

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138662269A>C (hg19) ; chr9:g.135770423A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770423A>C , CM000671.2:g.135770423A>C	GRCh38
NC_000009.11:g.138662269A>C , CM000671.1:g.138662269A>C	GRCh37
NC_000009.10:g.137802090A>C	NCBI36
NG_033070.1:g.73239A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1745A>C MANE Select	ENSP00000360822.2:p.Tyr582Ser
ENST00000674572.1:c.1586A>C	ENSP00000501742.1:p.Tyr529Ser
ENST00000675090.1:c.1493A>C	ENSP00000501833.1:p.Tyr498Ser
ENST00000675399.1:c.1493A>C	ENSP00000501932.1:p.Tyr498Ser
ENST00000676421.1:c.1502A>C	ENSP00000502322.1:p.Tyr501Ser
ENST00000263604.5:c.1646A>C	ENSP00000263604.4:p.Tyr549Ser
ENST00000371757.6:c.1745A>C	ENSP00000360822.2:p.Tyr582Ser
ENST00000460750.5:c.*1355A>C	ENSP00000418777.1:n.*1355A>C
ENST00000486577.6:c.1628A>C	ENSP00000417578.3:p.Tyr543Ser
ENST00000487664.5:c.1745A>C	ENSP00000417851.2:p.Tyr582Ser
ENST00000488444.6:c.1688A>C	ENSP00000419007.3:p.Tyr563Ser
ENST00000490355.6:c.1688A>C	ENSP00000418003.3:p.Tyr563Ser
ENST00000490363.3:n.1564A>C
ENST00000491806.6:c.1688A>C	ENSP00000419086.3:p.Tyr563Ser
ENST00000628528.2:c.1610A>C	ENSP00000486374.1:p.Tyr537Ser
ENST00000630792.2:c.1586A>C	ENSP00000486486.1:p.Tyr529Ser
ENST00000631073.2:c.1688A>C	ENSP00000486130.1:p.Tyr563Ser
NM_001272003.1:c.1610A>C	NP_001258932.1:p.Tyr537Ser
NM_020822.2:c.1745A>C	NP_065873.2:p.Tyr582Ser
XM_011518877.1:c.1880A>C	XP_011517179.1:p.Tyr627Ser
XM_011518878.1:c.1889A>C	XP_011517180.1:p.Tyr630Ser
XM_011518879.1:c.1880A>C	XP_011517181.1:p.Tyr627Ser
XM_011518880.1:c.1646A>C	XP_011517182.1:p.Tyr549Ser
XM_011518881.1:c.1235A>C	XP_011517183.1:p.Tyr412Ser
XM_011518877.3:c.1880A>C	XP_011517179.1:p.Tyr627Ser
XM_011518878.3:c.1889A>C	XP_011517180.1:p.Tyr630Ser
XM_011518879.3:c.1880A>C	XP_011517181.1:p.Tyr627Ser
XM_011518881.3:c.1235A>C	XP_011517183.1:p.Tyr412Ser
XM_017014931.1:c.1679A>C	XP_016870420.1:p.Tyr560Ser
XM_017014932.1:c.1502A>C	XP_016870421.1:p.Tyr501Ser
XM_017014933.1:c.1235A>C	XP_016870422.1:p.Tyr412Ser
XM_024447617.1:c.1235A>C	XP_024303385.1:p.Tyr412Ser
XM_024447618.1:c.1235A>C	XP_024303386.1:p.Tyr412Ser
NM_020822.3:c.1745A>C MANE Select	NP_065873.2:p.Tyr582Ser
NM_001272003.2:c.1610A>C	NP_001258932.1:p.Tyr537Ser