Canonical Allele Identifier: CA1883884826

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775357_135775358delinsCA , CM000671.2:g.135775357_135775358delinsCA	GRCh38
NC_000009.11:g.138667203_138667204delinsCA , CM000671.1:g.138667203_138667204delinsCA	GRCh37
NC_000009.10:g.137807024_137807025delinsCA	NCBI36
NG_033070.1:g.78173_78174delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2291_2292delinsCA MANE Select	ENSP00000360822.2:p.Pro764=
ENST00000674572.1:c.2132_2133delinsCA	ENSP00000501742.1:p.Pro711=
ENST00000675090.1:c.2039_2040delinsCA	ENSP00000501833.1:p.Pro680=
ENST00000675399.1:c.2039_2040delinsCA	ENSP00000501932.1:p.Pro680=
ENST00000676421.1:c.2048_2049delinsCA	ENSP00000502322.1:p.Pro683=
ENST00000263604.5:c.2192_2193delinsCA	ENSP00000263604.4:p.Pro731=
ENST00000371757.6:c.2291_2292delinsCA	ENSP00000360822.2:p.Pro764=
ENST00000460750.5:c.*1901_*1902delinsCA	ENSP00000418777.1:n.*1901_*1902delinsCA
ENST00000486577.6:c.2174_2175delinsCA	ENSP00000417578.3:p.Pro725=
ENST00000487664.5:c.2291_2292delinsCA	ENSP00000417851.2:p.Pro764=
ENST00000488444.6:c.2234_2235delinsCA	ENSP00000419007.3:p.Pro745=
ENST00000490355.6:c.2228_2229delinsCA	ENSP00000418003.3:p.Pro743=
ENST00000490363.3:n.2110_2111delinsCA
ENST00000491806.6:c.2234_2235delinsCA	ENSP00000419086.3:p.Pro745=
ENST00000628528.2:c.2156_2157delinsCA	ENSP00000486374.1:p.Pro719=
ENST00000630792.2:c.2126_2127delinsCA	ENSP00000486486.1:p.Pro709=
ENST00000631073.2:c.2234_2235delinsCA	ENSP00000486130.1:p.Pro745=
ENST00000631193.1:c.140_141delinsCA	ENSP00000486830.1:p.Pro47=
NM_001272003.1:c.2156_2157delinsCA	NP_001258932.1:p.Pro719=
NM_020822.2:c.2291_2292delinsCA	NP_065873.2:p.Pro764=
XM_011518877.1:c.2426_2427delinsCA	XP_011517179.1:p.Pro809=
XM_011518878.1:c.2435_2436delinsCA	XP_011517180.1:p.Pro812=
XM_011518879.1:c.2426_2427delinsCA	XP_011517181.1:p.Pro809=
XM_011518880.1:c.2192_2193delinsCA	XP_011517182.1:p.Pro731=
XM_011518881.1:c.1781_1782delinsCA	XP_011517183.1:p.Pro594=
XM_011518877.3:c.2426_2427delinsCA	XP_011517179.1:p.Pro809=
XM_011518878.3:c.2435_2436delinsCA	XP_011517180.1:p.Pro812=
XM_011518879.3:c.2426_2427delinsCA	XP_011517181.1:p.Pro809=
XM_011518881.3:c.1781_1782delinsCA	XP_011517183.1:p.Pro594=
XM_017014931.1:c.2225_2226delinsCA	XP_016870420.1:p.Pro742=
XM_017014932.1:c.2048_2049delinsCA	XP_016870421.1:p.Pro683=
XM_017014933.1:c.1781_1782delinsCA	XP_016870422.1:p.Pro594=
XM_024447617.1:c.1781_1782delinsCA	XP_024303385.1:p.Pro594=
XM_024447618.1:c.1781_1782delinsCA	XP_024303386.1:p.Pro594=
NM_020822.3:c.2291_2292delinsCA MANE Select	NP_065873.2:p.Pro764=
NM_001272003.2:c.2156_2157delinsCA	NP_001258932.1:p.Pro719=