Canonical Allele Identifier: CA2579510815

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765580G>T , CM000671.2:g.135765580G>T	GRCh38
NC_000009.11:g.138657426G>T , CM000671.1:g.138657426G>T	GRCh37
NC_000009.10:g.137797247G>T	NCBI36
NG_033070.1:g.68396G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371757.7:c.1201-44G>T MANE Select	ENSP00000360822.2:n.1201-44G>T
ENST00000674572.1:c.1042-44G>T	ENSP00000501742.1:n.1042-44G>T
ENST00000675090.1:c.949-44G>T	ENSP00000501833.1:n.949-44G>T
ENST00000675399.1:c.949-44G>T	ENSP00000501932.1:n.949-44G>T
ENST00000676421.1:c.958-44G>T	ENSP00000502322.1:n.958-44G>T
ENST00000263604.5:c.1102-44G>T	ENSP00000263604.4:n.1102-44G>T
ENST00000371757.6:c.1201-44G>T	ENSP00000360822.2:n.1201-44G>T
ENST00000460750.5:c.*811-44G>T	ENSP00000418777.1:n.*811-44G>T
ENST00000486577.6:c.1084-44G>T	ENSP00000417578.3:n.1084-44G>T
ENST00000487664.5:c.1201-44G>T	ENSP00000417851.2:n.1201-44G>T
ENST00000488444.6:c.1144-44G>T	ENSP00000419007.3:n.1144-44G>T
ENST00000490355.6:c.1144-44G>T	ENSP00000418003.3:n.1144-44G>T
ENST00000490363.3:n.1020-44G>T
ENST00000491806.6:c.1144-44G>T	ENSP00000419086.3:n.1144-44G>T
ENST00000628528.2:c.1066-44G>T	ENSP00000486374.1:n.1066-44G>T
ENST00000630792.2:c.1042-44G>T	ENSP00000486486.1:n.1042-44G>T
ENST00000631073.2:c.1144-44G>T	ENSP00000486130.1:n.1144-44G>T
NM_001272003.1:c.1066-44G>T	NP_001258932.1:n.1066-44G>T
NM_020822.2:c.1201-44G>T	NP_065873.2:n.1201-44G>T
XM_011518877.1:c.1336-44G>T	XP_011517179.1:n.1336-44G>T
XM_011518878.1:c.1345-44G>T	XP_011517180.1:n.1345-44G>T
XM_011518879.1:c.1336-44G>T	XP_011517181.1:n.1336-44G>T
XM_011518880.1:c.1102-44G>T	XP_011517182.1:n.1102-44G>T
XM_011518881.1:c.691-44G>T	XP_011517183.1:n.691-44G>T
XM_011518877.3:c.1336-44G>T	XP_011517179.1:n.1336-44G>T
XM_011518878.3:c.1345-44G>T	XP_011517180.1:n.1345-44G>T
XM_011518879.3:c.1336-44G>T	XP_011517181.1:n.1336-44G>T
XM_011518881.3:c.691-44G>T	XP_011517183.1:n.691-44G>T
XM_017014931.1:c.1135-44G>T	XP_016870420.1:n.1135-44G>T
XM_017014932.1:c.958-44G>T	XP_016870421.1:n.958-44G>T
XM_017014933.1:c.691-44G>T	XP_016870422.1:n.691-44G>T
XM_024447617.1:c.691-44G>T	XP_024303385.1:n.691-44G>T
XM_024447618.1:c.691-44G>T	XP_024303386.1:n.691-44G>T
NM_020822.3:c.1201-44G>T MANE Select	NP_065873.2:n.1201-44G>T
NM_001272003.2:c.1066-44G>T	NP_001258932.1:n.1066-44G>T