Canonical Allele Identifier: CA375500111

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765108G>C , CM000671.2:g.135765108G>C	GRCh38
NC_000009.11:g.138656954G>C , CM000671.1:g.138656954G>C	GRCh37
NC_000009.10:g.137796775G>C	NCBI36
NG_033070.1:g.67924G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020822.3:c.1113G>C MANE Select	NP_065873.2:p.Glu371Asp
ENST00000371757.7:c.1113G>C MANE Select	ENSP00000360822.2:p.Glu371Asp
NM_001272003.1:c.978G>C	NP_001258932.1:p.Glu326Asp
NM_001272003.2:c.978G>C	NP_001258932.1:p.Glu326Asp
NM_020822.2:c.1113G>C	NP_065873.2:p.Glu371Asp
ENST00000263604.5:c.1014G>C	ENSP00000263604.4:p.Glu338Asp
ENST00000371757.6:c.1113G>C	ENSP00000360822.2:p.Glu371Asp
ENST00000460750.5:c.*723G>C	ENSP00000418777.1:n.*723G>C
ENST00000486577.6:c.996G>C	ENSP00000417578.3:p.Glu332Asp
ENST00000487664.5:c.1113G>C	ENSP00000417851.2:p.Glu371Asp
ENST00000488444.6:c.1056G>C	ENSP00000419007.3:p.Glu352Asp
ENST00000490355.6:c.1056G>C	ENSP00000418003.3:p.Glu352Asp
ENST00000490363.3:n.932G>C
ENST00000491806.6:c.1056G>C	ENSP00000419086.3:p.Glu352Asp
ENST00000628528.2:c.978G>C	ENSP00000486374.1:p.Glu326Asp
ENST00000630792.2:c.954G>C	ENSP00000486486.1:p.Glu318Asp
ENST00000631073.2:c.1056G>C	ENSP00000486130.1:p.Glu352Asp
ENST00000674572.1:c.954G>C	ENSP00000501742.1:p.Glu318Asp
ENST00000675090.1:c.861G>C	ENSP00000501833.1:p.Glu287Asp
ENST00000675399.1:c.861G>C	ENSP00000501932.1:p.Glu287Asp
ENST00000676421.1:c.870G>C	ENSP00000502322.1:p.Glu290Asp
XM_011518877.1:c.1248G>C	XP_011517179.1:p.Glu416Asp
XM_011518877.3:c.1248G>C	XP_011517179.1:p.Glu416Asp
XM_011518878.1:c.1257G>C	XP_011517180.1:p.Glu419Asp
XM_011518878.3:c.1257G>C	XP_011517180.1:p.Glu419Asp
XM_011518879.1:c.1248G>C	XP_011517181.1:p.Glu416Asp
XM_011518879.3:c.1248G>C	XP_011517181.1:p.Glu416Asp
XM_011518880.1:c.1014G>C	XP_011517182.1:p.Glu338Asp
XM_011518881.1:c.603G>C	XP_011517183.1:p.Glu201Asp
XM_011518881.3:c.603G>C	XP_011517183.1:p.Glu201Asp
XM_017014931.1:c.1047G>C	XP_016870420.1:p.Glu349Asp
XM_017014932.1:c.870G>C	XP_016870421.1:p.Glu290Asp
XM_017014933.1:c.603G>C	XP_016870422.1:p.Glu201Asp
XM_024447617.1:c.603G>C	XP_024303385.1:p.Glu201Asp
XM_024447618.1:c.603G>C	XP_024303386.1:p.Glu201Asp