Canonical Allele Identifier: CA1883872422
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135769968A= , CM000671.2:g.135769968A= GRCh38
NC_000009.11:g.138661814A= , CM000671.1:g.138661814A= GRCh37
NC_000009.10:g.137801635A= NCBI36
NG_033070.1:g.72784A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.1532A= MANE Select ENSP00000360822.2:p.Glu511=
ENST00000674572.1:c.1373A= ENSP00000501742.1:p.Glu458=
ENST00000675090.1:c.1280A= ENSP00000501833.1:p.Glu427=
ENST00000675399.1:c.1280A= ENSP00000501932.1:p.Glu427=
ENST00000676421.1:c.1289A= ENSP00000502322.1:p.Glu430=
ENST00000263604.5:c.1433A= ENSP00000263604.4:p.Glu478=
ENST00000371757.6:c.1532A= ENSP00000360822.2:p.Glu511=
ENST00000460750.5:c.*1142A= ENSP00000418777.1:n.*1142A=
ENST00000486577.6:c.1415A= ENSP00000417578.3:p.Glu472=
ENST00000487664.5:c.1532A= ENSP00000417851.2:p.Glu511=
ENST00000488444.6:c.1475A= ENSP00000419007.3:p.Glu492=
ENST00000490355.6:c.1475A= ENSP00000418003.3:p.Glu492=
ENST00000490363.3:n.1351A=
ENST00000491806.6:c.1475A= ENSP00000419086.3:p.Glu492=
ENST00000628528.2:c.1397A= ENSP00000486374.1:p.Glu466=
ENST00000630792.2:c.1373A= ENSP00000486486.1:p.Glu458=
ENST00000631073.2:c.1475A= ENSP00000486130.1:p.Glu492=
NM_001272003.1:c.1397A= NP_001258932.1:p.Glu466=
NM_020822.2:c.1532A= NP_065873.2:p.Glu511=
XM_011518877.1:c.1667A= XP_011517179.1:p.Glu556=
XM_011518878.1:c.1676A= XP_011517180.1:p.Glu559=
XM_011518879.1:c.1667A= XP_011517181.1:p.Glu556=
XM_011518880.1:c.1433A= XP_011517182.1:p.Glu478=
XM_011518881.1:c.1022A= XP_011517183.1:p.Glu341=
XM_011518877.3:c.1667A= XP_011517179.1:p.Glu556=
XM_011518878.3:c.1676A= XP_011517180.1:p.Glu559=
XM_011518879.3:c.1667A= XP_011517181.1:p.Glu556=
XM_011518881.3:c.1022A= XP_011517183.1:p.Glu341=
XM_017014931.1:c.1466A= XP_016870420.1:p.Glu489=
XM_017014932.1:c.1289A= XP_016870421.1:p.Glu430=
XM_017014933.1:c.1022A= XP_016870422.1:p.Glu341=
XM_024447617.1:c.1022A= XP_024303385.1:p.Glu341=
XM_024447618.1:c.1022A= XP_024303386.1:p.Glu341=
NM_020822.3:c.1532A= MANE Select NP_065873.2:p.Glu511=
NM_001272003.2:c.1397A= NP_001258932.1:p.Glu466=