Canonical Allele Identifier: CA3171542682
Community Standard Title: NM_020822.3(KCNT1):c.1199A= (p.Gln400=)
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135765194A= , CM000671.2:g.135765194A= GRCh38
NC_000009.11:g.138657040A= , CM000671.1:g.138657040A= GRCh37
NC_000009.10:g.137796861A= NCBI36
NG_033070.1:g.68010A=

Transcript Alleles

HGVS Amino-acid Change
NM_020822.3:c.1199A= MANE Select NP_065873.2:p.Gln400=
ENST00000371757.7:c.1199A= MANE Select ENSP00000360822.2:p.Gln400=
NM_001272003.1:c.1064A= NP_001258932.1:p.Gln355=
NM_001272003.2:c.1064A= NP_001258932.1:p.Gln355=
NM_020822.2:c.1199A= NP_065873.2:p.Gln400=
ENST00000263604.5:c.1100A= ENSP00000263604.4:p.Gln367=
ENST00000371757.6:c.1199A= ENSP00000360822.2:p.Gln400=
ENST00000460750.5:c.*809A= ENSP00000418777.1:n.*809A=
ENST00000486577.6:c.1082A= ENSP00000417578.3:p.Gln361=
ENST00000487664.5:c.1199A= ENSP00000417851.2:p.Gln400=
ENST00000488444.6:c.1142A= ENSP00000419007.3:p.Gln381=
ENST00000490355.6:c.1142A= ENSP00000418003.3:p.Gln381=
ENST00000490363.3:n.1018A=
ENST00000491806.6:c.1142A= ENSP00000419086.3:p.Gln381=
ENST00000628528.2:c.1064A= ENSP00000486374.1:p.Gln355=
ENST00000630792.2:c.1040A= ENSP00000486486.1:p.Gln347=
ENST00000631073.2:c.1142A= ENSP00000486130.1:p.Gln381=
ENST00000674572.1:c.1040A= ENSP00000501742.1:p.Gln347=
ENST00000675090.1:c.947A= ENSP00000501833.1:p.Gln316=
ENST00000675399.1:c.947A= ENSP00000501932.1:p.Gln316=
ENST00000676421.1:c.956A= ENSP00000502322.1:p.Gln319=
XM_011518877.1:c.1334A= XP_011517179.1:p.Gln445=
XM_011518877.3:c.1334A= XP_011517179.1:p.Gln445=
XM_011518878.1:c.1343A= XP_011517180.1:p.Gln448=
XM_011518878.3:c.1343A= XP_011517180.1:p.Gln448=
XM_011518879.1:c.1334A= XP_011517181.1:p.Gln445=
XM_011518879.3:c.1334A= XP_011517181.1:p.Gln445=
XM_011518880.1:c.1100A= XP_011517182.1:p.Gln367=
XM_011518881.1:c.689A= XP_011517183.1:p.Gln230=
XM_011518881.3:c.689A= XP_011517183.1:p.Gln230=
XM_017014931.1:c.1133A= XP_016870420.1:p.Gln378=
XM_017014932.1:c.956A= XP_016870421.1:p.Gln319=
XM_017014933.1:c.689A= XP_016870422.1:p.Gln230=
XM_024447617.1:c.689A= XP_024303385.1:p.Gln230=
XM_024447618.1:c.689A= XP_024303386.1:p.Gln230=