Canonical Allele Identifier: CA375499956

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138656916T>A (hg19) ; chr9:g.135765070T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765070T>A , CM000671.2:g.135765070T>A	GRCh38
NC_000009.11:g.138656916T>A , CM000671.1:g.138656916T>A	GRCh37
NC_000009.10:g.137796737T>A	NCBI36
NG_033070.1:g.67886T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371757.7:c.1075T>A MANE Select	ENSP00000360822.2:p.Ser359Thr
ENST00000674572.1:c.916T>A	ENSP00000501742.1:p.Ser306Thr
ENST00000675090.1:c.823T>A	ENSP00000501833.1:p.Ser275Thr
ENST00000675399.1:c.823T>A	ENSP00000501932.1:p.Ser275Thr
ENST00000676421.1:c.832T>A	ENSP00000502322.1:p.Ser278Thr
ENST00000263604.5:c.976T>A	ENSP00000263604.4:p.Ser326Thr
ENST00000371757.6:c.1075T>A	ENSP00000360822.2:p.Ser359Thr
ENST00000460750.5:c.*685T>A	ENSP00000418777.1:n.*685T>A
ENST00000486577.6:c.958T>A	ENSP00000417578.3:p.Ser320Thr
ENST00000487664.5:c.1075T>A	ENSP00000417851.2:p.Ser359Thr
ENST00000488444.6:c.1018T>A	ENSP00000419007.3:p.Ser340Thr
ENST00000490355.6:c.1018T>A	ENSP00000418003.3:p.Ser340Thr
ENST00000490363.3:n.894T>A
ENST00000491806.6:c.1018T>A	ENSP00000419086.3:p.Ser340Thr
ENST00000628528.2:c.940T>A	ENSP00000486374.1:p.Ser314Thr
ENST00000630792.2:c.916T>A	ENSP00000486486.1:p.Ser306Thr
ENST00000631073.2:c.1018T>A	ENSP00000486130.1:p.Ser340Thr
NM_001272003.1:c.940T>A	NP_001258932.1:p.Ser314Thr
NM_020822.2:c.1075T>A	NP_065873.2:p.Ser359Thr
XM_011518877.1:c.1210T>A	XP_011517179.1:p.Ser404Thr
XM_011518878.1:c.1219T>A	XP_011517180.1:p.Ser407Thr
XM_011518879.1:c.1210T>A	XP_011517181.1:p.Ser404Thr
XM_011518880.1:c.976T>A	XP_011517182.1:p.Ser326Thr
XM_011518881.1:c.565T>A	XP_011517183.1:p.Ser189Thr
XM_011518877.3:c.1210T>A	XP_011517179.1:p.Ser404Thr
XM_011518878.3:c.1219T>A	XP_011517180.1:p.Ser407Thr
XM_011518879.3:c.1210T>A	XP_011517181.1:p.Ser404Thr
XM_011518881.3:c.565T>A	XP_011517183.1:p.Ser189Thr
XM_017014931.1:c.1009T>A	XP_016870420.1:p.Ser337Thr
XM_017014932.1:c.832T>A	XP_016870421.1:p.Ser278Thr
XM_017014933.1:c.565T>A	XP_016870422.1:p.Ser189Thr
XM_024447617.1:c.565T>A	XP_024303385.1:p.Ser189Thr
XM_024447618.1:c.565T>A	XP_024303386.1:p.Ser189Thr
NM_020822.3:c.1075T>A MANE Select	NP_065873.2:p.Ser359Thr
NM_001272003.2:c.940T>A	NP_001258932.1:p.Ser314Thr