Canonical Allele Identifier: CA375494725
Gene: KCNT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135750116C>A , CM000671.2:g.135750116C>A GRCh38
NC_000009.11:g.138641962C>A , CM000671.1:g.138641962C>A GRCh37
NC_000009.10:g.137781783C>A NCBI36
NG_033070.1:g.52932C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.273C>A MANE Select ENSP00000360822.2:p.Tyr91Ter
ENST00000637018.1:n.78C>A
ENST00000638123.1:n.8C>A
ENST00000674572.1:c.114C>A ENSP00000501742.1:p.Tyr38Ter
ENST00000675090.1:c.21C>A ENSP00000501833.1:p.Tyr7Ter
ENST00000675399.1:c.21C>A ENSP00000501932.1:p.Tyr7Ter
ENST00000676421.1:c.21C>A ENSP00000502322.1:p.Tyr7Ter
ENST00000263604.5:c.174C>A ENSP00000263604.4:p.Tyr58Ter
ENST00000371757.6:c.273C>A ENSP00000360822.2:p.Tyr91Ter
ENST00000460750.5:c.273C>A ENSP00000418777.1:p.Tyr91Ter
ENST00000473941.5:c.114C>A ENSP00000420764.1:p.Tyr38Ter
ENST00000486577.6:c.156C>A ENSP00000417578.3:p.Tyr52Ter
ENST00000487664.5:c.273C>A ENSP00000417851.2:p.Tyr91Ter
ENST00000488444.6:c.216C>A ENSP00000419007.3:p.Tyr72Ter
ENST00000490355.6:c.216C>A ENSP00000418003.3:p.Tyr72Ter
ENST00000491806.6:c.216C>A ENSP00000419086.3:p.Tyr72Ter
ENST00000628528.2:c.129C>A ENSP00000486374.1:p.Tyr43Ter
ENST00000630792.2:c.114C>A ENSP00000486486.1:p.Tyr38Ter
ENST00000631073.2:c.216C>A ENSP00000486130.1:p.Tyr72Ter
NM_001272003.1:c.129C>A NP_001258932.1:p.Tyr43Ter
NM_020822.2:c.273C>A NP_065873.2:p.Tyr91Ter
XM_011518877.1:c.408C>A XP_011517179.1:p.Tyr136Ter
XM_011518878.1:c.408C>A XP_011517180.1:p.Tyr136Ter
XM_011518879.1:c.408C>A XP_011517181.1:p.Tyr136Ter
XM_011518880.1:c.174C>A XP_011517182.1:p.Tyr58Ter
XM_011518877.3:c.408C>A XP_011517179.1:p.Tyr136Ter
XM_011518878.3:c.408C>A XP_011517180.1:p.Tyr136Ter
XM_011518879.3:c.408C>A XP_011517181.1:p.Tyr136Ter
XM_017014931.1:c.298C>A XP_016870420.1:p.Arg100Ser
XM_017014932.1:c.21C>A XP_016870421.1:p.Tyr7Ter
XM_017014933.1:c.-147C>A XP_016870422.1:n.-147C>A
XM_024447617.1:c.-247C>A XP_024303385.1:n.-247C>A
XM_024447618.1:c.-247C>A XP_024303386.1:n.-247C>A
NM_020822.3:c.273C>A MANE Select NP_065873.2:p.Tyr91Ter
NM_001272003.2:c.129C>A NP_001258932.1:p.Tyr43Ter