Canonical Allele Identifier: CA1883873778
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135770501G= , CM000671.2:g.135770501G= GRCh38
NC_000009.11:g.138662347G= , CM000671.1:g.138662347G= GRCh37
NC_000009.10:g.137802168G= NCBI36
NG_033070.1:g.73317G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.1769+54G= MANE Select ENSP00000360822.2:n.1769+54G=
ENST00000674572.1:c.1610+54G= ENSP00000501742.1:n.1610+54G=
ENST00000675090.1:c.1517+54G= ENSP00000501833.1:n.1517+54G=
ENST00000675399.1:c.1517+54G= ENSP00000501932.1:n.1517+54G=
ENST00000676421.1:c.1526+54G= ENSP00000502322.1:n.1526+54G=
ENST00000263604.5:c.1670+54G= ENSP00000263604.4:n.1670+54G=
ENST00000371757.6:c.1769+54G= ENSP00000360822.2:n.1769+54G=
ENST00000460750.5:c.*1379+54G= ENSP00000418777.1:n.*1379+54G=
ENST00000486577.6:c.1652+54G= ENSP00000417578.3:n.1652+54G=
ENST00000487664.5:c.1769+54G= ENSP00000417851.2:n.1769+54G=
ENST00000488444.6:c.1712+54G= ENSP00000419007.3:n.1712+54G=
ENST00000490355.6:c.1712+54G= ENSP00000418003.3:n.1712+54G=
ENST00000490363.3:n.1588+54G=
ENST00000491806.6:c.1712+54G= ENSP00000419086.3:n.1712+54G=
ENST00000628528.2:c.1634+54G= ENSP00000486374.1:n.1634+54G=
ENST00000630792.2:c.1610+54G= ENSP00000486486.1:n.1610+54G=
ENST00000631073.2:c.1712+54G= ENSP00000486130.1:n.1712+54G=
NM_001272003.1:c.1634+54G= NP_001258932.1:n.1634+54G=
NM_020822.2:c.1769+54G= NP_065873.2:n.1769+54G=
XM_011518877.1:c.1904+54G= XP_011517179.1:n.1904+54G=
XM_011518878.1:c.1913+54G= XP_011517180.1:n.1913+54G=
XM_011518879.1:c.1904+54G= XP_011517181.1:n.1904+54G=
XM_011518880.1:c.1670+54G= XP_011517182.1:n.1670+54G=
XM_011518881.1:c.1259+54G= XP_011517183.1:n.1259+54G=
XM_011518877.3:c.1904+54G= XP_011517179.1:n.1904+54G=
XM_011518878.3:c.1913+54G= XP_011517180.1:n.1913+54G=
XM_011518879.3:c.1904+54G= XP_011517181.1:n.1904+54G=
XM_011518881.3:c.1259+54G= XP_011517183.1:n.1259+54G=
XM_017014931.1:c.1703+54G= XP_016870420.1:n.1703+54G=
XM_017014932.1:c.1526+54G= XP_016870421.1:n.1526+54G=
XM_017014933.1:c.1259+54G= XP_016870422.1:n.1259+54G=
XM_024447617.1:c.1259+54G= XP_024303385.1:n.1259+54G=
XM_024447618.1:c.1259+54G= XP_024303386.1:n.1259+54G=
NM_020822.3:c.1769+54G= MANE Select NP_065873.2:n.1769+54G=
NM_001272003.2:c.1634+54G= NP_001258932.1:n.1634+54G=