Canonical Allele Identifier: CA375499831

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138656889G>C (hg19) ; chr9:g.135765043G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765043G>C , CM000671.2:g.135765043G>C	GRCh38
NC_000009.11:g.138656889G>C , CM000671.1:g.138656889G>C	GRCh37
NC_000009.10:g.137796710G>C	NCBI36
NG_033070.1:g.67859G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1048G>C MANE Select	ENSP00000360822.2:p.Val350Leu
ENST00000674572.1:c.889G>C	ENSP00000501742.1:p.Val297Leu
ENST00000675090.1:c.796G>C	ENSP00000501833.1:p.Val266Leu
ENST00000675399.1:c.796G>C	ENSP00000501932.1:p.Val266Leu
ENST00000676421.1:c.805G>C	ENSP00000502322.1:p.Val269Leu
ENST00000263604.5:c.949G>C	ENSP00000263604.4:p.Val317Leu
ENST00000371757.6:c.1048G>C	ENSP00000360822.2:p.Val350Leu
ENST00000460750.5:c.*658G>C	ENSP00000418777.1:n.*658G>C
ENST00000486577.6:c.931G>C	ENSP00000417578.3:p.Val311Leu
ENST00000487664.5:c.1048G>C	ENSP00000417851.2:p.Val350Leu
ENST00000488444.6:c.991G>C	ENSP00000419007.3:p.Val331Leu
ENST00000490355.6:c.991G>C	ENSP00000418003.3:p.Val331Leu
ENST00000490363.3:n.867G>C
ENST00000491806.6:c.991G>C	ENSP00000419086.3:p.Val331Leu
ENST00000628528.2:c.913G>C	ENSP00000486374.1:p.Val305Leu
ENST00000630792.2:c.889G>C	ENSP00000486486.1:p.Val297Leu
ENST00000631073.2:c.991G>C	ENSP00000486130.1:p.Val331Leu
NM_001272003.1:c.913G>C	NP_001258932.1:p.Val305Leu
NM_020822.2:c.1048G>C	NP_065873.2:p.Val350Leu
XM_011518877.1:c.1183G>C	XP_011517179.1:p.Val395Leu
XM_011518878.1:c.1192G>C	XP_011517180.1:p.Val398Leu
XM_011518879.1:c.1183G>C	XP_011517181.1:p.Val395Leu
XM_011518880.1:c.949G>C	XP_011517182.1:p.Val317Leu
XM_011518881.1:c.538G>C	XP_011517183.1:p.Val180Leu
XM_011518877.3:c.1183G>C	XP_011517179.1:p.Val395Leu
XM_011518878.3:c.1192G>C	XP_011517180.1:p.Val398Leu
XM_011518879.3:c.1183G>C	XP_011517181.1:p.Val395Leu
XM_011518881.3:c.538G>C	XP_011517183.1:p.Val180Leu
XM_017014931.1:c.982G>C	XP_016870420.1:p.Val328Leu
XM_017014932.1:c.805G>C	XP_016870421.1:p.Val269Leu
XM_017014933.1:c.538G>C	XP_016870422.1:p.Val180Leu
XM_024447617.1:c.538G>C	XP_024303385.1:p.Val180Leu
XM_024447618.1:c.538G>C	XP_024303386.1:p.Val180Leu
NM_020822.3:c.1048G>C MANE Select	NP_065873.2:p.Val350Leu
NM_001272003.2:c.913G>C	NP_001258932.1:p.Val305Leu