Canonical Allele Identifier: CA1883873809

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135778781G= , CM000671.2:g.135778781G=	GRCh38
NC_000009.11:g.138670627G= , CM000671.1:g.138670627G=	GRCh37
NC_000009.10:g.137810448G=	NCBI36
NG_033070.1:g.81597G=

Transcript Alleles

HGVS	Amino-acid Change
NM_020822.3:c.2688G= MANE Select	NP_065873.2:p.Met896=
ENST00000371757.7:c.2688G= MANE Select	ENSP00000360822.2:p.Met896=
NM_001272003.1:c.2553G=	NP_001258932.1:p.Met851=
NM_001272003.2:c.2553G=	NP_001258932.1:p.Met851=
NM_020822.2:c.2688G=	NP_065873.2:p.Met896=
ENST00000263604.5:c.2589G=	ENSP00000263604.4:p.Met863=
ENST00000371757.6:c.2688G=	ENSP00000360822.2:p.Met896=
ENST00000460750.5:c.*2298G=	ENSP00000418777.1:n.*2298G=
ENST00000486577.6:c.2571G=	ENSP00000417578.3:p.Met857=
ENST00000487664.5:c.2688G=	ENSP00000417851.2:p.Met896=
ENST00000488444.6:c.2631G=	ENSP00000419007.3:p.Met877=
ENST00000490355.6:c.2625G=	ENSP00000418003.3:p.Met875=
ENST00000490363.3:n.2507G=
ENST00000491806.6:c.2631G=	ENSP00000419086.3:p.Met877=
ENST00000628528.2:c.2553G=	ENSP00000486374.1:p.Met851=
ENST00000630792.2:c.2523G=	ENSP00000486486.1:p.Met841=
ENST00000631073.2:c.2631G=	ENSP00000486130.1:p.Met877=
ENST00000631193.1:c.554G=	ENSP00000486830.1:n.554G=
ENST00000674572.1:c.2529G=	ENSP00000501742.1:p.Met843=
ENST00000675090.1:c.2436G=	ENSP00000501833.1:p.Met812=
ENST00000675102.1:n.1222G=
ENST00000675399.1:c.2436G=	ENSP00000501932.1:p.Met812=
ENST00000676421.1:c.2445G=	ENSP00000502322.1:p.Met815=
XM_011518877.1:c.2823G=	XP_011517179.1:p.Met941=
XM_011518877.3:c.2823G=	XP_011517179.1:p.Met941=
XM_011518878.1:c.2832G=	XP_011517180.1:p.Met944=
XM_011518878.3:c.2832G=	XP_011517180.1:p.Met944=
XM_011518879.1:c.2823G=	XP_011517181.1:p.Met941=
XM_011518879.3:c.2823G=	XP_011517181.1:p.Met941=
XM_011518880.1:c.2589G=	XP_011517182.1:p.Met863=
XM_011518881.1:c.2178G=	XP_011517183.1:p.Met726=
XM_011518881.3:c.2178G=	XP_011517183.1:p.Met726=
XM_017014931.1:c.2622G=	XP_016870420.1:p.Met874=
XM_017014932.1:c.2445G=	XP_016870421.1:p.Met815=
XM_017014933.1:c.2178G=	XP_016870422.1:p.Met726=
XM_024447617.1:c.2178G=	XP_024303385.1:p.Met726=
XM_024447618.1:c.2178G=	XP_024303386.1:p.Met726=