Canonical Allele Identifier: CA375501300
Gene: KCNT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135765666C>A , CM000671.2:g.135765666C>A GRCh38
NC_000009.11:g.138657512C>A , CM000671.1:g.138657512C>A GRCh37
NC_000009.10:g.137797333C>A NCBI36
NG_033070.1:g.68482C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.1243C>A MANE Select ENSP00000360822.2:p.Gln415Lys
ENST00000674572.1:c.1084C>A ENSP00000501742.1:p.Gln362Lys
ENST00000675090.1:c.991C>A ENSP00000501833.1:p.Gln331Lys
ENST00000675399.1:c.991C>A ENSP00000501932.1:p.Gln331Lys
ENST00000676421.1:c.1000C>A ENSP00000502322.1:p.Gln334Lys
ENST00000263604.5:c.1144C>A ENSP00000263604.4:p.Gln382Lys
ENST00000371757.6:c.1243C>A ENSP00000360822.2:p.Gln415Lys
ENST00000460750.5:c.*853C>A ENSP00000418777.1:n.*853C>A
ENST00000486577.6:c.1126C>A ENSP00000417578.3:p.Gln376Lys
ENST00000487664.5:c.1243C>A ENSP00000417851.2:p.Gln415Lys
ENST00000488444.6:c.1186C>A ENSP00000419007.3:p.Gln396Lys
ENST00000490355.6:c.1186C>A ENSP00000418003.3:p.Gln396Lys
ENST00000490363.3:n.1062C>A
ENST00000491806.6:c.1186C>A ENSP00000419086.3:p.Gln396Lys
ENST00000628528.2:c.1108C>A ENSP00000486374.1:p.Gln370Lys
ENST00000630792.2:c.1084C>A ENSP00000486486.1:p.Gln362Lys
ENST00000631073.2:c.1186C>A ENSP00000486130.1:p.Gln396Lys
NM_001272003.1:c.1108C>A NP_001258932.1:p.Gln370Lys
NM_020822.2:c.1243C>A NP_065873.2:p.Gln415Lys
XM_011518877.1:c.1378C>A XP_011517179.1:p.Gln460Lys
XM_011518878.1:c.1387C>A XP_011517180.1:p.Gln463Lys
XM_011518879.1:c.1378C>A XP_011517181.1:p.Gln460Lys
XM_011518880.1:c.1144C>A XP_011517182.1:p.Gln382Lys
XM_011518881.1:c.733C>A XP_011517183.1:p.Gln245Lys
XM_011518877.3:c.1378C>A XP_011517179.1:p.Gln460Lys
XM_011518878.3:c.1387C>A XP_011517180.1:p.Gln463Lys
XM_011518879.3:c.1378C>A XP_011517181.1:p.Gln460Lys
XM_011518881.3:c.733C>A XP_011517183.1:p.Gln245Lys
XM_017014931.1:c.1177C>A XP_016870420.1:p.Gln393Lys
XM_017014932.1:c.1000C>A XP_016870421.1:p.Gln334Lys
XM_017014933.1:c.733C>A XP_016870422.1:p.Gln245Lys
XM_024447617.1:c.733C>A XP_024303385.1:p.Gln245Lys
XM_024447618.1:c.733C>A XP_024303386.1:p.Gln245Lys
NM_020822.3:c.1243C>A MANE Select NP_065873.2:p.Gln415Lys
NM_001272003.2:c.1108C>A NP_001258932.1:p.Gln370Lys