Canonical Allele Identifier: CA2692518970

Gene: KCNT1

Linked Data

• gnomAD v4: 9-135770510-A-ACCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770513_135770514insGCCC , CM000671.2:g.135770513_135770514insGCCC	GRCh38
NC_000009.11:g.138662359_138662360insGCCC , CM000671.1:g.138662359_138662360insGCCC	GRCh37
NC_000009.10:g.137802180_137802181insGCCC	NCBI36
NG_033070.1:g.73329_73330insGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1769+66_1769+67insGCCC MANE Select	ENSP00000360822.2:n.1769+66_1769+67insGCCC
ENST00000674572.1:c.1610+66_1610+67insGCCC	ENSP00000501742.1:n.1610+66_1610+67insGCCC
ENST00000675090.1:c.1517+66_1517+67insGCCC	ENSP00000501833.1:n.1517+66_1517+67insGCCC
ENST00000675399.1:c.1517+66_1517+67insGCCC	ENSP00000501932.1:n.1517+66_1517+67insGCCC
ENST00000676421.1:c.1526+66_1526+67insGCCC	ENSP00000502322.1:n.1526+66_1526+67insGCCC
ENST00000263604.5:c.1670+66_1670+67insGCCC	ENSP00000263604.4:n.1670+66_1670+67insGCCC
ENST00000371757.6:c.1769+66_1769+67insGCCC	ENSP00000360822.2:n.1769+66_1769+67insGCCC
ENST00000460750.5:c.*1379+66_*1379+67insGCCC	ENSP00000418777.1:n.*1379+66_*1379+67insGCCC
ENST00000486577.6:c.1652+66_1652+67insGCCC	ENSP00000417578.3:n.1652+66_1652+67insGCCC
ENST00000487664.5:c.1769+66_1769+67insGCCC	ENSP00000417851.2:n.1769+66_1769+67insGCCC
ENST00000488444.6:c.1712+66_1712+67insGCCC	ENSP00000419007.3:n.1712+66_1712+67insGCCC
ENST00000490355.6:c.1712+66_1712+67insGCCC	ENSP00000418003.3:n.1712+66_1712+67insGCCC
ENST00000490363.3:n.1588+66_1588+67insGCCC
ENST00000491806.6:c.1712+66_1712+67insGCCC	ENSP00000419086.3:n.1712+66_1712+67insGCCC
ENST00000628528.2:c.1634+66_1634+67insGCCC	ENSP00000486374.1:n.1634+66_1634+67insGCCC
ENST00000630792.2:c.1610+66_1610+67insGCCC	ENSP00000486486.1:n.1610+66_1610+67insGCCC
ENST00000631073.2:c.1712+66_1712+67insGCCC	ENSP00000486130.1:n.1712+66_1712+67insGCCC
NM_001272003.1:c.1634+66_1634+67insGCCC	NP_001258932.1:n.1634+66_1634+67insGCCC
NM_020822.2:c.1769+66_1769+67insGCCC	NP_065873.2:n.1769+66_1769+67insGCCC
XM_011518877.1:c.1904+66_1904+67insGCCC	XP_011517179.1:n.1904+66_1904+67insGCCC
XM_011518878.1:c.1913+66_1913+67insGCCC	XP_011517180.1:n.1913+66_1913+67insGCCC
XM_011518879.1:c.1904+66_1904+67insGCCC	XP_011517181.1:n.1904+66_1904+67insGCCC
XM_011518880.1:c.1670+66_1670+67insGCCC	XP_011517182.1:n.1670+66_1670+67insGCCC
XM_011518881.1:c.1259+66_1259+67insGCCC	XP_011517183.1:n.1259+66_1259+67insGCCC
XM_011518877.3:c.1904+66_1904+67insGCCC	XP_011517179.1:n.1904+66_1904+67insGCCC
XM_011518878.3:c.1913+66_1913+67insGCCC	XP_011517180.1:n.1913+66_1913+67insGCCC
XM_011518879.3:c.1904+66_1904+67insGCCC	XP_011517181.1:n.1904+66_1904+67insGCCC
XM_011518881.3:c.1259+66_1259+67insGCCC	XP_011517183.1:n.1259+66_1259+67insGCCC
XM_017014931.1:c.1703+66_1703+67insGCCC	XP_016870420.1:n.1703+66_1703+67insGCCC
XM_017014932.1:c.1526+66_1526+67insGCCC	XP_016870421.1:n.1526+66_1526+67insGCCC
XM_017014933.1:c.1259+66_1259+67insGCCC	XP_016870422.1:n.1259+66_1259+67insGCCC
XM_024447617.1:c.1259+66_1259+67insGCCC	XP_024303385.1:n.1259+66_1259+67insGCCC
XM_024447618.1:c.1259+66_1259+67insGCCC	XP_024303386.1:n.1259+66_1259+67insGCCC
NM_020822.3:c.1769+66_1769+67insGCCC MANE Select	NP_065873.2:n.1769+66_1769+67insGCCC
NM_001272003.2:c.1634+66_1634+67insGCCC	NP_001258932.1:n.1634+66_1634+67insGCCC