Canonical Allele Identifier: CA375505833
Gene: KCNT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135769952G>C , CM000671.2:g.135769952G>C GRCh38
NC_000009.11:g.138661798G>C , CM000671.1:g.138661798G>C GRCh37
NC_000009.10:g.137801619G>C NCBI36
NG_033070.1:g.72768G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371757.7:c.1516G>C MANE Select ENSP00000360822.2:p.Val506Leu
ENST00000674572.1:c.1357G>C ENSP00000501742.1:p.Val453Leu
ENST00000675090.1:c.1264G>C ENSP00000501833.1:p.Val422Leu
ENST00000675399.1:c.1264G>C ENSP00000501932.1:p.Val422Leu
ENST00000676421.1:c.1273G>C ENSP00000502322.1:p.Val425Leu
ENST00000263604.5:c.1417G>C ENSP00000263604.4:p.Val473Leu
ENST00000371757.6:c.1516G>C ENSP00000360822.2:p.Val506Leu
ENST00000460750.5:c.*1126G>C ENSP00000418777.1:n.*1126G>C
ENST00000486577.6:c.1399G>C ENSP00000417578.3:p.Val467Leu
ENST00000487664.5:c.1516G>C ENSP00000417851.2:p.Val506Leu
ENST00000488444.6:c.1459G>C ENSP00000419007.3:p.Val487Leu
ENST00000490355.6:c.1459G>C ENSP00000418003.3:p.Val487Leu
ENST00000490363.3:n.1335G>C
ENST00000491806.6:c.1459G>C ENSP00000419086.3:p.Val487Leu
ENST00000628528.2:c.1381G>C ENSP00000486374.1:p.Val461Leu
ENST00000630792.2:c.1357G>C ENSP00000486486.1:p.Val453Leu
ENST00000631073.2:c.1459G>C ENSP00000486130.1:p.Val487Leu
NM_001272003.1:c.1381G>C NP_001258932.1:p.Val461Leu
NM_020822.2:c.1516G>C NP_065873.2:p.Val506Leu
XM_011518877.1:c.1651G>C XP_011517179.1:p.Val551Leu
XM_011518878.1:c.1660G>C XP_011517180.1:p.Val554Leu
XM_011518879.1:c.1651G>C XP_011517181.1:p.Val551Leu
XM_011518880.1:c.1417G>C XP_011517182.1:p.Val473Leu
XM_011518881.1:c.1006G>C XP_011517183.1:p.Val336Leu
XM_011518877.3:c.1651G>C XP_011517179.1:p.Val551Leu
XM_011518878.3:c.1660G>C XP_011517180.1:p.Val554Leu
XM_011518879.3:c.1651G>C XP_011517181.1:p.Val551Leu
XM_011518881.3:c.1006G>C XP_011517183.1:p.Val336Leu
XM_017014931.1:c.1450G>C XP_016870420.1:p.Val484Leu
XM_017014932.1:c.1273G>C XP_016870421.1:p.Val425Leu
XM_017014933.1:c.1006G>C XP_016870422.1:p.Val336Leu
XM_024447617.1:c.1006G>C XP_024303385.1:p.Val336Leu
XM_024447618.1:c.1006G>C XP_024303386.1:p.Val336Leu
NM_020822.3:c.1516G>C MANE Select NP_065873.2:p.Val506Leu
NM_001272003.2:c.1381G>C NP_001258932.1:p.Val461Leu