Canonical Allele Identifier: CA1883873666
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135770441A= , CM000671.2:g.135770441A= GRCh38
NC_000009.11:g.138662287A= , CM000671.1:g.138662287A= GRCh37
NC_000009.10:g.137802108A= NCBI36
NG_033070.1:g.73257A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.1763A= MANE Select ENSP00000360822.2:p.His588=
ENST00000674572.1:c.1604A= ENSP00000501742.1:p.His535=
ENST00000675090.1:c.1511A= ENSP00000501833.1:p.His504=
ENST00000675399.1:c.1511A= ENSP00000501932.1:p.His504=
ENST00000676421.1:c.1520A= ENSP00000502322.1:p.His507=
ENST00000263604.5:c.1664A= ENSP00000263604.4:p.His555=
ENST00000371757.6:c.1763A= ENSP00000360822.2:p.His588=
ENST00000460750.5:c.*1373A= ENSP00000418777.1:n.*1373A=
ENST00000486577.6:c.1646A= ENSP00000417578.3:p.His549=
ENST00000487664.5:c.1763A= ENSP00000417851.2:p.His588=
ENST00000488444.6:c.1706A= ENSP00000419007.3:p.His569=
ENST00000490355.6:c.1706A= ENSP00000418003.3:p.His569=
ENST00000490363.3:n.1582A=
ENST00000491806.6:c.1706A= ENSP00000419086.3:p.His569=
ENST00000628528.2:c.1628A= ENSP00000486374.1:p.His543=
ENST00000630792.2:c.1604A= ENSP00000486486.1:p.His535=
ENST00000631073.2:c.1706A= ENSP00000486130.1:p.His569=
NM_001272003.1:c.1628A= NP_001258932.1:p.His543=
NM_020822.2:c.1763A= NP_065873.2:p.His588=
XM_011518877.1:c.1898A= XP_011517179.1:p.His633=
XM_011518878.1:c.1907A= XP_011517180.1:p.His636=
XM_011518879.1:c.1898A= XP_011517181.1:p.His633=
XM_011518880.1:c.1664A= XP_011517182.1:p.His555=
XM_011518881.1:c.1253A= XP_011517183.1:p.His418=
XM_011518877.3:c.1898A= XP_011517179.1:p.His633=
XM_011518878.3:c.1907A= XP_011517180.1:p.His636=
XM_011518879.3:c.1898A= XP_011517181.1:p.His633=
XM_011518881.3:c.1253A= XP_011517183.1:p.His418=
XM_017014931.1:c.1697A= XP_016870420.1:p.His566=
XM_017014932.1:c.1520A= XP_016870421.1:p.His507=
XM_017014933.1:c.1253A= XP_016870422.1:p.His418=
XM_024447617.1:c.1253A= XP_024303385.1:p.His418=
XM_024447618.1:c.1253A= XP_024303386.1:p.His418=
NM_020822.3:c.1763A= MANE Select NP_065873.2:p.His588=
NM_001272003.2:c.1628A= NP_001258932.1:p.His543=