Canonical Allele Identifier: CA467698532

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138662225T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770379T>G , CM000671.2:g.135770379T>G	GRCh38
NC_000009.11:g.138662225T>G , CM000671.1:g.138662225T>G	GRCh37
NC_000009.10:g.137802046T>G	NCBI36
NG_033070.1:g.73195T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1701T>G MANE Select	ENSP00000360822.2:p.Gly567=
ENST00000674572.1:c.1542T>G	ENSP00000501742.1:p.Gly514=
ENST00000675090.1:c.1449T>G	ENSP00000501833.1:p.Gly483=
ENST00000675399.1:c.1449T>G	ENSP00000501932.1:p.Gly483=
ENST00000676421.1:c.1458T>G	ENSP00000502322.1:p.Gly486=
ENST00000263604.5:c.1602T>G	ENSP00000263604.4:p.Gly534=
ENST00000371757.6:c.1701T>G	ENSP00000360822.2:p.Gly567=
ENST00000460750.5:c.*1311T>G	ENSP00000418777.1:n.*1311T>G
ENST00000486577.6:c.1584T>G	ENSP00000417578.3:p.Gly528=
ENST00000487664.5:c.1701T>G	ENSP00000417851.2:p.Gly567=
ENST00000488444.6:c.1644T>G	ENSP00000419007.3:p.Gly548=
ENST00000490355.6:c.1644T>G	ENSP00000418003.3:p.Gly548=
ENST00000490363.3:n.1520T>G
ENST00000491806.6:c.1644T>G	ENSP00000419086.3:p.Gly548=
ENST00000628528.2:c.1566T>G	ENSP00000486374.1:p.Gly522=
ENST00000630792.2:c.1542T>G	ENSP00000486486.1:p.Gly514=
ENST00000631073.2:c.1644T>G	ENSP00000486130.1:p.Gly548=
NM_001272003.1:c.1566T>G	NP_001258932.1:p.Gly522=
NM_020822.2:c.1701T>G	NP_065873.2:p.Gly567=
XM_011518877.1:c.1836T>G	XP_011517179.1:p.Gly612=
XM_011518878.1:c.1845T>G	XP_011517180.1:p.Gly615=
XM_011518879.1:c.1836T>G	XP_011517181.1:p.Gly612=
XM_011518880.1:c.1602T>G	XP_011517182.1:p.Gly534=
XM_011518881.1:c.1191T>G	XP_011517183.1:p.Gly397=
XM_011518877.3:c.1836T>G	XP_011517179.1:p.Gly612=
XM_011518878.3:c.1845T>G	XP_011517180.1:p.Gly615=
XM_011518879.3:c.1836T>G	XP_011517181.1:p.Gly612=
XM_011518881.3:c.1191T>G	XP_011517183.1:p.Gly397=
XM_017014931.1:c.1635T>G	XP_016870420.1:p.Gly545=
XM_017014932.1:c.1458T>G	XP_016870421.1:p.Gly486=
XM_017014933.1:c.1191T>G	XP_016870422.1:p.Gly397=
XM_024447617.1:c.1191T>G	XP_024303385.1:p.Gly397=
XM_024447618.1:c.1191T>G	XP_024303386.1:p.Gly397=
NM_020822.3:c.1701T>G MANE Select	NP_065873.2:p.Gly567=
NM_001272003.2:c.1566T>G	NP_001258932.1:p.Gly522=