Canonical Allele Identifier: CA860991743
Gene: KCNT1 HGNC NCBI

Linked Data

dbSNP Id: rs1445471318

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135775245_135775255dup , CM000671.2:g.135775245_135775255dup GRCh38
NC_000009.11:g.138667091_138667101dup , CM000671.1:g.138667091_138667101dup GRCh37
NC_000009.10:g.137806912_137806922dup NCBI36
NG_033070.1:g.78061_78071dup

Transcript Alleles

HGVS Amino-acid change
ENST00000371757.7:c.2244-65_2244-55dup MANE Select ENSP00000360822.2:n.2244-65_2244-55dup
ENST00000674572.1:c.2085-65_2085-55dup ENSP00000501742.1:n.2085-65_2085-55dup
ENST00000675090.1:c.1992-65_1992-55dup ENSP00000501833.1:n.1992-65_1992-55dup
ENST00000675399.1:c.1992-65_1992-55dup ENSP00000501932.1:n.1992-65_1992-55dup
ENST00000676421.1:c.2001-65_2001-55dup ENSP00000502322.1:n.2001-65_2001-55dup
ENST00000263604.5:c.2145-65_2145-55dup ENSP00000263604.4:n.2145-65_2145-55dup
ENST00000371757.6:c.2244-65_2244-55dup ENSP00000360822.2:n.2244-65_2244-55dup
ENST00000460750.5:c.*1854-65_*1854-55dup ENSP00000418777.1:n.*1854-65_*1854-55dup
ENST00000486577.6:c.2127-65_2127-55dup ENSP00000417578.3:n.2127-65_2127-55dup
ENST00000487664.5:c.2244-65_2244-55dup ENSP00000417851.2:n.2244-65_2244-55dup
ENST00000488444.6:c.2187-65_2187-55dup ENSP00000419007.3:n.2187-65_2187-55dup
ENST00000490355.6:c.2181-65_2181-55dup ENSP00000418003.3:n.2181-65_2181-55dup
ENST00000490363.3:n.2063-65_2063-55dup
ENST00000491806.6:c.2187-65_2187-55dup ENSP00000419086.3:n.2187-65_2187-55dup
ENST00000628528.2:c.2109-65_2109-55dup ENSP00000486374.1:n.2109-65_2109-55dup
ENST00000630792.2:c.2079-65_2079-55dup ENSP00000486486.1:n.2079-65_2079-55dup
ENST00000631073.2:c.2187-65_2187-55dup ENSP00000486130.1:n.2187-65_2187-55dup
ENST00000631193.1:c.93-65_93-55dup ENSP00000486830.1:n.93-65_93-55dup
NM_001272003.1:c.2109-65_2109-55dup NP_001258932.1:n.2109-65_2109-55dup
NM_020822.2:c.2244-65_2244-55dup NP_065873.2:n.2244-65_2244-55dup
XM_011518877.1:c.2379-65_2379-55dup XP_011517179.1:n.2379-65_2379-55dup
XM_011518878.1:c.2388-65_2388-55dup XP_011517180.1:n.2388-65_2388-55dup
XM_011518879.1:c.2379-65_2379-55dup XP_011517181.1:n.2379-65_2379-55dup
XM_011518880.1:c.2145-65_2145-55dup XP_011517182.1:n.2145-65_2145-55dup
XM_011518881.1:c.1734-65_1734-55dup XP_011517183.1:n.1734-65_1734-55dup
XM_011518877.3:c.2379-65_2379-55dup XP_011517179.1:n.2379-65_2379-55dup
XM_011518878.3:c.2388-65_2388-55dup XP_011517180.1:n.2388-65_2388-55dup
XM_011518879.3:c.2379-65_2379-55dup XP_011517181.1:n.2379-65_2379-55dup
XM_011518881.3:c.1734-65_1734-55dup XP_011517183.1:n.1734-65_1734-55dup
XM_017014931.1:c.2178-65_2178-55dup XP_016870420.1:n.2178-65_2178-55dup
XM_017014932.1:c.2001-65_2001-55dup XP_016870421.1:n.2001-65_2001-55dup
XM_017014933.1:c.1734-65_1734-55dup XP_016870422.1:n.1734-65_1734-55dup
XM_024447617.1:c.1734-65_1734-55dup XP_024303385.1:n.1734-65_1734-55dup
XM_024447618.1:c.1734-65_1734-55dup XP_024303386.1:n.1734-65_1734-55dup
NM_020822.3:c.2244-65_2244-55dup MANE Select NP_065873.2:n.2244-65_2244-55dup
NM_001272003.2:c.2109-65_2109-55dup NP_001258932.1:n.2109-65_2109-55dup