Canonical Allele Identifier: CA375506590

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138662227A>C (hg19) ; chr9:g.135770381A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770381A>C , CM000671.2:g.135770381A>C	GRCh38
NC_000009.11:g.138662227A>C , CM000671.1:g.138662227A>C	GRCh37
NC_000009.10:g.137802048A>C	NCBI36
NG_033070.1:g.73197A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1703A>C MANE Select	ENSP00000360822.2:p.Asp568Ala
ENST00000674572.1:c.1544A>C	ENSP00000501742.1:p.Asp515Ala
ENST00000675090.1:c.1451A>C	ENSP00000501833.1:p.Asp484Ala
ENST00000675399.1:c.1451A>C	ENSP00000501932.1:p.Asp484Ala
ENST00000676421.1:c.1460A>C	ENSP00000502322.1:p.Asp487Ala
ENST00000263604.5:c.1604A>C	ENSP00000263604.4:p.Asp535Ala
ENST00000371757.6:c.1703A>C	ENSP00000360822.2:p.Asp568Ala
ENST00000460750.5:c.*1313A>C	ENSP00000418777.1:n.*1313A>C
ENST00000486577.6:c.1586A>C	ENSP00000417578.3:p.Asp529Ala
ENST00000487664.5:c.1703A>C	ENSP00000417851.2:p.Asp568Ala
ENST00000488444.6:c.1646A>C	ENSP00000419007.3:p.Asp549Ala
ENST00000490355.6:c.1646A>C	ENSP00000418003.3:p.Asp549Ala
ENST00000490363.3:n.1522A>C
ENST00000491806.6:c.1646A>C	ENSP00000419086.3:p.Asp549Ala
ENST00000628528.2:c.1568A>C	ENSP00000486374.1:p.Asp523Ala
ENST00000630792.2:c.1544A>C	ENSP00000486486.1:p.Asp515Ala
ENST00000631073.2:c.1646A>C	ENSP00000486130.1:p.Asp549Ala
NM_001272003.1:c.1568A>C	NP_001258932.1:p.Asp523Ala
NM_020822.2:c.1703A>C	NP_065873.2:p.Asp568Ala
XM_011518877.1:c.1838A>C	XP_011517179.1:p.Asp613Ala
XM_011518878.1:c.1847A>C	XP_011517180.1:p.Asp616Ala
XM_011518879.1:c.1838A>C	XP_011517181.1:p.Asp613Ala
XM_011518880.1:c.1604A>C	XP_011517182.1:p.Asp535Ala
XM_011518881.1:c.1193A>C	XP_011517183.1:p.Asp398Ala
XM_011518877.3:c.1838A>C	XP_011517179.1:p.Asp613Ala
XM_011518878.3:c.1847A>C	XP_011517180.1:p.Asp616Ala
XM_011518879.3:c.1838A>C	XP_011517181.1:p.Asp613Ala
XM_011518881.3:c.1193A>C	XP_011517183.1:p.Asp398Ala
XM_017014931.1:c.1637A>C	XP_016870420.1:p.Asp546Ala
XM_017014932.1:c.1460A>C	XP_016870421.1:p.Asp487Ala
XM_017014933.1:c.1193A>C	XP_016870422.1:p.Asp398Ala
XM_024447617.1:c.1193A>C	XP_024303385.1:p.Asp398Ala
XM_024447618.1:c.1193A>C	XP_024303386.1:p.Asp398Ala
NM_020822.3:c.1703A>C MANE Select	NP_065873.2:p.Asp568Ala
NM_001272003.2:c.1568A>C	NP_001258932.1:p.Asp523Ala