Canonical Allele Identifier: CA467698116

Gene: KCNT1

Linked Data

• dbSNP Id: rs781506115
• MyVariant Identifiers: chr9:g.138657035G>C (hg19) ; chr9:g.135765189G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765189G>C , CM000671.2:g.135765189G>C	GRCh38
NC_000009.11:g.138657035G>C , CM000671.1:g.138657035G>C	GRCh37
NC_000009.10:g.137796856G>C	NCBI36
NG_033070.1:g.68005G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1194G>C MANE Select	ENSP00000360822.2:p.Arg398=
ENST00000674572.1:c.1035G>C	ENSP00000501742.1:p.Arg345=
ENST00000675090.1:c.942G>C	ENSP00000501833.1:p.Arg314=
ENST00000675399.1:c.942G>C	ENSP00000501932.1:p.Arg314=
ENST00000676421.1:c.951G>C	ENSP00000502322.1:p.Arg317=
ENST00000263604.5:c.1095G>C	ENSP00000263604.4:p.Arg365=
ENST00000371757.6:c.1194G>C	ENSP00000360822.2:p.Arg398=
ENST00000460750.5:c.*804G>C	ENSP00000418777.1:n.*804G>C
ENST00000486577.6:c.1077G>C	ENSP00000417578.3:p.Arg359=
ENST00000487664.5:c.1194G>C	ENSP00000417851.2:p.Arg398=
ENST00000488444.6:c.1137G>C	ENSP00000419007.3:p.Arg379=
ENST00000490355.6:c.1137G>C	ENSP00000418003.3:p.Arg379=
ENST00000490363.3:n.1013G>C
ENST00000491806.6:c.1137G>C	ENSP00000419086.3:p.Arg379=
ENST00000628528.2:c.1059G>C	ENSP00000486374.1:p.Arg353=
ENST00000630792.2:c.1035G>C	ENSP00000486486.1:p.Arg345=
ENST00000631073.2:c.1137G>C	ENSP00000486130.1:p.Arg379=
NM_001272003.1:c.1059G>C	NP_001258932.1:p.Arg353=
NM_020822.2:c.1194G>C	NP_065873.2:p.Arg398=
XM_011518877.1:c.1329G>C	XP_011517179.1:p.Arg443=
XM_011518878.1:c.1338G>C	XP_011517180.1:p.Arg446=
XM_011518879.1:c.1329G>C	XP_011517181.1:p.Arg443=
XM_011518880.1:c.1095G>C	XP_011517182.1:p.Arg365=
XM_011518881.1:c.684G>C	XP_011517183.1:p.Arg228=
XM_011518877.3:c.1329G>C	XP_011517179.1:p.Arg443=
XM_011518878.3:c.1338G>C	XP_011517180.1:p.Arg446=
XM_011518879.3:c.1329G>C	XP_011517181.1:p.Arg443=
XM_011518881.3:c.684G>C	XP_011517183.1:p.Arg228=
XM_017014931.1:c.1128G>C	XP_016870420.1:p.Arg376=
XM_017014932.1:c.951G>C	XP_016870421.1:p.Arg317=
XM_017014933.1:c.684G>C	XP_016870422.1:p.Arg228=
XM_024447617.1:c.684G>C	XP_024303385.1:p.Arg228=
XM_024447618.1:c.684G>C	XP_024303386.1:p.Arg228=
NM_020822.3:c.1194G>C MANE Select	NP_065873.2:p.Arg398=
NM_001272003.2:c.1059G>C	NP_001258932.1:p.Arg353=