Canonical Allele Identifier: CA1883843222

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135750115A= , CM000671.2:g.135750115A=	GRCh38
NC_000009.11:g.138641961A= , CM000671.1:g.138641961A=	GRCh37
NC_000009.10:g.137781782A=	NCBI36
NG_033070.1:g.52931A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.272A= MANE Select	ENSP00000360822.2:p.Tyr91=
ENST00000637018.1:n.77A=
ENST00000638123.1:n.7A=
ENST00000674572.1:c.113A=	ENSP00000501742.1:p.Tyr38=
ENST00000675090.1:c.20A=	ENSP00000501833.1:p.Tyr7=
ENST00000675399.1:c.20A=	ENSP00000501932.1:p.Tyr7=
ENST00000676421.1:c.20A=	ENSP00000502322.1:p.Tyr7=
ENST00000263604.5:c.173A=	ENSP00000263604.4:p.Tyr58=
ENST00000371757.6:c.272A=	ENSP00000360822.2:p.Tyr91=
ENST00000460750.5:c.272A=	ENSP00000418777.1:p.Tyr91=
ENST00000473941.5:c.113A=	ENSP00000420764.1:p.Tyr38=
ENST00000486577.6:c.155A=	ENSP00000417578.3:p.Tyr52=
ENST00000487664.5:c.272A=	ENSP00000417851.2:p.Tyr91=
ENST00000488444.6:c.215A=	ENSP00000419007.3:p.Tyr72=
ENST00000490355.6:c.215A=	ENSP00000418003.3:p.Tyr72=
ENST00000491806.6:c.215A=	ENSP00000419086.3:p.Tyr72=
ENST00000628528.2:c.128A=	ENSP00000486374.1:p.Tyr43=
ENST00000630792.2:c.113A=	ENSP00000486486.1:p.Tyr38=
ENST00000631073.2:c.215A=	ENSP00000486130.1:p.Tyr72=
NM_001272003.1:c.128A=	NP_001258932.1:p.Tyr43=
NM_020822.2:c.272A=	NP_065873.2:p.Tyr91=
XM_011518877.1:c.407A=	XP_011517179.1:p.Tyr136=
XM_011518878.1:c.407A=	XP_011517180.1:p.Tyr136=
XM_011518879.1:c.407A=	XP_011517181.1:p.Tyr136=
XM_011518880.1:c.173A=	XP_011517182.1:p.Tyr58=
XM_011518877.3:c.407A=	XP_011517179.1:p.Tyr136=
XM_011518878.3:c.407A=	XP_011517180.1:p.Tyr136=
XM_011518879.3:c.407A=	XP_011517181.1:p.Tyr136=
XM_017014931.1:c.297A=	XP_016870420.1:p.Leu99=
XM_017014932.1:c.20A=	XP_016870421.1:p.Tyr7=
XM_017014933.1:c.-148A=	XP_016870422.1:n.-148A=
XM_024447617.1:c.-248A=	XP_024303385.1:n.-248A=
XM_024447618.1:c.-248A=	XP_024303386.1:n.-248A=
NM_020822.3:c.272A= MANE Select	NP_065873.2:p.Tyr91=
NM_001272003.2:c.128A=	NP_001258932.1:p.Tyr43=