Canonical Allele Identifier: CA375499806

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138656883G>C (hg19) ; chr9:g.135765037G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765037G>C , CM000671.2:g.135765037G>C	GRCh38
NC_000009.11:g.138656883G>C , CM000671.1:g.138656883G>C	GRCh37
NC_000009.10:g.137796704G>C	NCBI36
NG_033070.1:g.67853G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371757.7:c.1042G>C MANE Select	ENSP00000360822.2:p.Glu348Gln
ENST00000674572.1:c.883G>C	ENSP00000501742.1:p.Glu295Gln
ENST00000675090.1:c.790G>C	ENSP00000501833.1:p.Glu264Gln
ENST00000675399.1:c.790G>C	ENSP00000501932.1:p.Glu264Gln
ENST00000676421.1:c.799G>C	ENSP00000502322.1:p.Glu267Gln
ENST00000263604.5:c.943G>C	ENSP00000263604.4:p.Glu315Gln
ENST00000371757.6:c.1042G>C	ENSP00000360822.2:p.Glu348Gln
ENST00000460750.5:c.*652G>C	ENSP00000418777.1:n.*652G>C
ENST00000486577.6:c.925G>C	ENSP00000417578.3:p.Glu309Gln
ENST00000487664.5:c.1042G>C	ENSP00000417851.2:p.Glu348Gln
ENST00000488444.6:c.985G>C	ENSP00000419007.3:p.Glu329Gln
ENST00000490355.6:c.985G>C	ENSP00000418003.3:p.Glu329Gln
ENST00000490363.3:n.861G>C
ENST00000491806.6:c.985G>C	ENSP00000419086.3:p.Glu329Gln
ENST00000628528.2:c.907G>C	ENSP00000486374.1:p.Glu303Gln
ENST00000630792.2:c.883G>C	ENSP00000486486.1:p.Glu295Gln
ENST00000631073.2:c.985G>C	ENSP00000486130.1:p.Glu329Gln
NM_001272003.1:c.907G>C	NP_001258932.1:p.Glu303Gln
NM_020822.2:c.1042G>C	NP_065873.2:p.Glu348Gln
XM_011518877.1:c.1177G>C	XP_011517179.1:p.Glu393Gln
XM_011518878.1:c.1186G>C	XP_011517180.1:p.Glu396Gln
XM_011518879.1:c.1177G>C	XP_011517181.1:p.Glu393Gln
XM_011518880.1:c.943G>C	XP_011517182.1:p.Glu315Gln
XM_011518881.1:c.532G>C	XP_011517183.1:p.Glu178Gln
XM_011518877.3:c.1177G>C	XP_011517179.1:p.Glu393Gln
XM_011518878.3:c.1186G>C	XP_011517180.1:p.Glu396Gln
XM_011518879.3:c.1177G>C	XP_011517181.1:p.Glu393Gln
XM_011518881.3:c.532G>C	XP_011517183.1:p.Glu178Gln
XM_017014931.1:c.976G>C	XP_016870420.1:p.Glu326Gln
XM_017014932.1:c.799G>C	XP_016870421.1:p.Glu267Gln
XM_017014933.1:c.532G>C	XP_016870422.1:p.Glu178Gln
XM_024447617.1:c.532G>C	XP_024303385.1:p.Glu178Gln
XM_024447618.1:c.532G>C	XP_024303386.1:p.Glu178Gln
NM_020822.3:c.1042G>C MANE Select	NP_065873.2:p.Glu348Gln
NM_001272003.2:c.907G>C	NP_001258932.1:p.Glu303Gln