Canonical Allele Identifier: CA467698130

Gene: KCNT1

Linked Data

• gnomAD v4: 9-135765641-C-A
• MyVariant Identifiers: chr9:g.138657487C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765641C>A , CM000671.2:g.135765641C>A	GRCh38
NC_000009.11:g.138657487C>A , CM000671.1:g.138657487C>A	GRCh37
NC_000009.10:g.137797308C>A	NCBI36
NG_033070.1:g.68457C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371757.7:c.1218C>A MANE Select	ENSP00000360822.2:p.Ile406=
ENST00000674572.1:c.1059C>A	ENSP00000501742.1:p.Ile353=
ENST00000675090.1:c.966C>A	ENSP00000501833.1:p.Ile322=
ENST00000675399.1:c.966C>A	ENSP00000501932.1:p.Ile322=
ENST00000676421.1:c.975C>A	ENSP00000502322.1:p.Ile325=
ENST00000263604.5:c.1119C>A	ENSP00000263604.4:p.Ile373=
ENST00000371757.6:c.1218C>A	ENSP00000360822.2:p.Ile406=
ENST00000460750.5:c.*828C>A	ENSP00000418777.1:n.*828C>A
ENST00000486577.6:c.1101C>A	ENSP00000417578.3:p.Ile367=
ENST00000487664.5:c.1218C>A	ENSP00000417851.2:p.Ile406=
ENST00000488444.6:c.1161C>A	ENSP00000419007.3:p.Ile387=
ENST00000490355.6:c.1161C>A	ENSP00000418003.3:p.Ile387=
ENST00000490363.3:n.1037C>A
ENST00000491806.6:c.1161C>A	ENSP00000419086.3:p.Ile387=
ENST00000628528.2:c.1083C>A	ENSP00000486374.1:p.Ile361=
ENST00000630792.2:c.1059C>A	ENSP00000486486.1:p.Ile353=
ENST00000631073.2:c.1161C>A	ENSP00000486130.1:p.Ile387=
NM_001272003.1:c.1083C>A	NP_001258932.1:p.Ile361=
NM_020822.2:c.1218C>A	NP_065873.2:p.Ile406=
XM_011518877.1:c.1353C>A	XP_011517179.1:p.Ile451=
XM_011518878.1:c.1362C>A	XP_011517180.1:p.Ile454=
XM_011518879.1:c.1353C>A	XP_011517181.1:p.Ile451=
XM_011518880.1:c.1119C>A	XP_011517182.1:p.Ile373=
XM_011518881.1:c.708C>A	XP_011517183.1:p.Ile236=
XM_011518877.3:c.1353C>A	XP_011517179.1:p.Ile451=
XM_011518878.3:c.1362C>A	XP_011517180.1:p.Ile454=
XM_011518879.3:c.1353C>A	XP_011517181.1:p.Ile451=
XM_011518881.3:c.708C>A	XP_011517183.1:p.Ile236=
XM_017014931.1:c.1152C>A	XP_016870420.1:p.Ile384=
XM_017014932.1:c.975C>A	XP_016870421.1:p.Ile325=
XM_017014933.1:c.708C>A	XP_016870422.1:p.Ile236=
XM_024447617.1:c.708C>A	XP_024303385.1:p.Ile236=
XM_024447618.1:c.708C>A	XP_024303386.1:p.Ile236=
NM_020822.3:c.1218C>A MANE Select	NP_065873.2:p.Ile406=
NM_001272003.2:c.1083C>A	NP_001258932.1:p.Ile361=