Canonical Allele Identifier: CA467698592

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138662291G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770445G>A , CM000671.2:g.135770445G>A	GRCh38
NC_000009.11:g.138662291G>A , CM000671.1:g.138662291G>A	GRCh37
NC_000009.10:g.137802112G>A	NCBI36
NG_033070.1:g.73261G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1767G>A MANE Select	ENSP00000360822.2:p.Lys589=
ENST00000674572.1:c.1608G>A	ENSP00000501742.1:p.Lys536=
ENST00000675090.1:c.1515G>A	ENSP00000501833.1:p.Lys505=
ENST00000675399.1:c.1515G>A	ENSP00000501932.1:p.Lys505=
ENST00000676421.1:c.1524G>A	ENSP00000502322.1:p.Lys508=
ENST00000263604.5:c.1668G>A	ENSP00000263604.4:p.Lys556=
ENST00000371757.6:c.1767G>A	ENSP00000360822.2:p.Lys589=
ENST00000460750.5:c.*1377G>A	ENSP00000418777.1:n.*1377G>A
ENST00000486577.6:c.1650G>A	ENSP00000417578.3:p.Lys550=
ENST00000487664.5:c.1767G>A	ENSP00000417851.2:p.Lys589=
ENST00000488444.6:c.1710G>A	ENSP00000419007.3:p.Lys570=
ENST00000490355.6:c.1710G>A	ENSP00000418003.3:p.Lys570=
ENST00000490363.3:n.1586G>A
ENST00000491806.6:c.1710G>A	ENSP00000419086.3:p.Lys570=
ENST00000628528.2:c.1632G>A	ENSP00000486374.1:p.Lys544=
ENST00000630792.2:c.1608G>A	ENSP00000486486.1:p.Lys536=
ENST00000631073.2:c.1710G>A	ENSP00000486130.1:p.Lys570=
NM_001272003.1:c.1632G>A	NP_001258932.1:p.Lys544=
NM_020822.2:c.1767G>A	NP_065873.2:p.Lys589=
XM_011518877.1:c.1902G>A	XP_011517179.1:p.Lys634=
XM_011518878.1:c.1911G>A	XP_011517180.1:p.Lys637=
XM_011518879.1:c.1902G>A	XP_011517181.1:p.Lys634=
XM_011518880.1:c.1668G>A	XP_011517182.1:p.Lys556=
XM_011518881.1:c.1257G>A	XP_011517183.1:p.Lys419=
XM_011518877.3:c.1902G>A	XP_011517179.1:p.Lys634=
XM_011518878.3:c.1911G>A	XP_011517180.1:p.Lys637=
XM_011518879.3:c.1902G>A	XP_011517181.1:p.Lys634=
XM_011518881.3:c.1257G>A	XP_011517183.1:p.Lys419=
XM_017014931.1:c.1701G>A	XP_016870420.1:p.Lys567=
XM_017014932.1:c.1524G>A	XP_016870421.1:p.Lys508=
XM_017014933.1:c.1257G>A	XP_016870422.1:p.Lys419=
XM_024447617.1:c.1257G>A	XP_024303385.1:p.Lys419=
XM_024447618.1:c.1257G>A	XP_024303386.1:p.Lys419=
NM_020822.3:c.1767G>A MANE Select	NP_065873.2:p.Lys589=
NM_001272003.2:c.1632G>A	NP_001258932.1:p.Lys544=