Canonical Allele Identifier: CA2692518145

Gene: KCNT1

Linked Data

• gnomAD v4: 9-135769861-A-AGCACCTTCAGGAAGTGAGCAGGTACTGTGGGGGAGGAGAGAGCCGGCAGAGCGGCAGGTGGACCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135769862_135769927dup , CM000671.2:g.135769862_135769927dup	GRCh38
NC_000009.11:g.138661708_138661773dup , CM000671.1:g.138661708_138661773dup	GRCh37
NC_000009.10:g.137801529_137801594dup	NCBI36
NG_033070.1:g.72678_72743dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000371757.7:c.1511-85_1511-20dup MANE Select	ENSP00000360822.2:n.1511-85_1511-20dup
ENST00000674572.1:c.1352-85_1352-20dup	ENSP00000501742.1:n.1352-85_1352-20dup
ENST00000675090.1:c.1259-85_1259-20dup	ENSP00000501833.1:n.1259-85_1259-20dup
ENST00000675399.1:c.1259-85_1259-20dup	ENSP00000501932.1:n.1259-85_1259-20dup
ENST00000676421.1:c.1268-85_1268-20dup	ENSP00000502322.1:n.1268-85_1268-20dup
ENST00000263604.5:c.1412-85_1412-20dup	ENSP00000263604.4:n.1412-85_1412-20dup
ENST00000371757.6:c.1511-85_1511-20dup	ENSP00000360822.2:n.1511-85_1511-20dup
ENST00000460750.5:c.*1121-85_*1121-20dup	ENSP00000418777.1:n.*1121-85_*1121-20dup
ENST00000486577.6:c.1394-85_1394-20dup	ENSP00000417578.3:n.1394-85_1394-20dup
ENST00000487664.5:c.1511-85_1511-20dup	ENSP00000417851.2:n.1511-85_1511-20dup
ENST00000488444.6:c.1454-85_1454-20dup	ENSP00000419007.3:n.1454-85_1454-20dup
ENST00000490355.6:c.1454-85_1454-20dup	ENSP00000418003.3:n.1454-85_1454-20dup
ENST00000490363.3:n.1330-85_1330-20dup
ENST00000491806.6:c.1454-85_1454-20dup	ENSP00000419086.3:n.1454-85_1454-20dup
ENST00000628528.2:c.1376-85_1376-20dup	ENSP00000486374.1:n.1376-85_1376-20dup
ENST00000630792.2:c.1352-85_1352-20dup	ENSP00000486486.1:n.1352-85_1352-20dup
ENST00000631073.2:c.1454-85_1454-20dup	ENSP00000486130.1:n.1454-85_1454-20dup
NM_001272003.1:c.1376-85_1376-20dup	NP_001258932.1:n.1376-85_1376-20dup
NM_020822.2:c.1511-85_1511-20dup	NP_065873.2:n.1511-85_1511-20dup
XM_011518877.1:c.1646-85_1646-20dup	XP_011517179.1:n.1646-85_1646-20dup
XM_011518878.1:c.1655-85_1655-20dup	XP_011517180.1:n.1655-85_1655-20dup
XM_011518879.1:c.1646-85_1646-20dup	XP_011517181.1:n.1646-85_1646-20dup
XM_011518880.1:c.1412-85_1412-20dup	XP_011517182.1:n.1412-85_1412-20dup
XM_011518881.1:c.1001-85_1001-20dup	XP_011517183.1:n.1001-85_1001-20dup
XM_011518877.3:c.1646-85_1646-20dup	XP_011517179.1:n.1646-85_1646-20dup
XM_011518878.3:c.1655-85_1655-20dup	XP_011517180.1:n.1655-85_1655-20dup
XM_011518879.3:c.1646-85_1646-20dup	XP_011517181.1:n.1646-85_1646-20dup
XM_011518881.3:c.1001-85_1001-20dup	XP_011517183.1:n.1001-85_1001-20dup
XM_017014931.1:c.1445-85_1445-20dup	XP_016870420.1:n.1445-85_1445-20dup
XM_017014932.1:c.1268-85_1268-20dup	XP_016870421.1:n.1268-85_1268-20dup
XM_017014933.1:c.1001-85_1001-20dup	XP_016870422.1:n.1001-85_1001-20dup
XM_024447617.1:c.1001-85_1001-20dup	XP_024303385.1:n.1001-85_1001-20dup
XM_024447618.1:c.1001-85_1001-20dup	XP_024303386.1:n.1001-85_1001-20dup
NM_020822.3:c.1511-85_1511-20dup MANE Select	NP_065873.2:n.1511-85_1511-20dup
NM_001272003.2:c.1376-85_1376-20dup	NP_001258932.1:n.1376-85_1376-20dup