Canonical Allele Identifier: CA375499909

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138656905A>T (hg19) ; chr9:g.135765059A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765059A>T , CM000671.2:g.135765059A>T	GRCh38
NC_000009.11:g.138656905A>T , CM000671.1:g.138656905A>T	GRCh37
NC_000009.10:g.137796726A>T	NCBI36
NG_033070.1:g.67875A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371757.7:c.1064A>T MANE Select	ENSP00000360822.2:p.Glu355Val
ENST00000674572.1:c.905A>T	ENSP00000501742.1:p.Glu302Val
ENST00000675090.1:c.812A>T	ENSP00000501833.1:p.Glu271Val
ENST00000675399.1:c.812A>T	ENSP00000501932.1:p.Glu271Val
ENST00000676421.1:c.821A>T	ENSP00000502322.1:p.Glu274Val
ENST00000263604.5:c.965A>T	ENSP00000263604.4:p.Glu322Val
ENST00000371757.6:c.1064A>T	ENSP00000360822.2:p.Glu355Val
ENST00000460750.5:c.*674A>T	ENSP00000418777.1:n.*674A>T
ENST00000486577.6:c.947A>T	ENSP00000417578.3:p.Glu316Val
ENST00000487664.5:c.1064A>T	ENSP00000417851.2:p.Glu355Val
ENST00000488444.6:c.1007A>T	ENSP00000419007.3:p.Glu336Val
ENST00000490355.6:c.1007A>T	ENSP00000418003.3:p.Glu336Val
ENST00000490363.3:n.883A>T
ENST00000491806.6:c.1007A>T	ENSP00000419086.3:p.Glu336Val
ENST00000628528.2:c.929A>T	ENSP00000486374.1:p.Glu310Val
ENST00000630792.2:c.905A>T	ENSP00000486486.1:p.Glu302Val
ENST00000631073.2:c.1007A>T	ENSP00000486130.1:p.Glu336Val
NM_001272003.1:c.929A>T	NP_001258932.1:p.Glu310Val
NM_020822.2:c.1064A>T	NP_065873.2:p.Glu355Val
XM_011518877.1:c.1199A>T	XP_011517179.1:p.Glu400Val
XM_011518878.1:c.1208A>T	XP_011517180.1:p.Glu403Val
XM_011518879.1:c.1199A>T	XP_011517181.1:p.Glu400Val
XM_011518880.1:c.965A>T	XP_011517182.1:p.Glu322Val
XM_011518881.1:c.554A>T	XP_011517183.1:p.Glu185Val
XM_011518877.3:c.1199A>T	XP_011517179.1:p.Glu400Val
XM_011518878.3:c.1208A>T	XP_011517180.1:p.Glu403Val
XM_011518879.3:c.1199A>T	XP_011517181.1:p.Glu400Val
XM_011518881.3:c.554A>T	XP_011517183.1:p.Glu185Val
XM_017014931.1:c.998A>T	XP_016870420.1:p.Glu333Val
XM_017014932.1:c.821A>T	XP_016870421.1:p.Glu274Val
XM_017014933.1:c.554A>T	XP_016870422.1:p.Glu185Val
XM_024447617.1:c.554A>T	XP_024303385.1:p.Glu185Val
XM_024447618.1:c.554A>T	XP_024303386.1:p.Glu185Val
NM_020822.3:c.1064A>T MANE Select	NP_065873.2:p.Glu355Val
NM_001272003.2:c.929A>T	NP_001258932.1:p.Glu310Val