Canonical Allele Identifier: CA1883872442
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135769978C= , CM000671.2:g.135769978C= GRCh38
NC_000009.11:g.138661824C= , CM000671.1:g.138661824C= GRCh37
NC_000009.10:g.137801645C= NCBI36
NG_033070.1:g.72794C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.1542C= MANE Select ENSP00000360822.2:p.Tyr514=
ENST00000674572.1:c.1383C= ENSP00000501742.1:p.Tyr461=
ENST00000675090.1:c.1290C= ENSP00000501833.1:p.Tyr430=
ENST00000675399.1:c.1290C= ENSP00000501932.1:p.Tyr430=
ENST00000676421.1:c.1299C= ENSP00000502322.1:p.Tyr433=
ENST00000263604.5:c.1443C= ENSP00000263604.4:p.Tyr481=
ENST00000371757.6:c.1542C= ENSP00000360822.2:p.Tyr514=
ENST00000460750.5:c.*1152C= ENSP00000418777.1:n.*1152C=
ENST00000486577.6:c.1425C= ENSP00000417578.3:p.Tyr475=
ENST00000487664.5:c.1542C= ENSP00000417851.2:p.Tyr514=
ENST00000488444.6:c.1485C= ENSP00000419007.3:p.Tyr495=
ENST00000490355.6:c.1485C= ENSP00000418003.3:p.Tyr495=
ENST00000490363.3:n.1361C=
ENST00000491806.6:c.1485C= ENSP00000419086.3:p.Tyr495=
ENST00000628528.2:c.1407C= ENSP00000486374.1:p.Tyr469=
ENST00000630792.2:c.1383C= ENSP00000486486.1:p.Tyr461=
ENST00000631073.2:c.1485C= ENSP00000486130.1:p.Tyr495=
NM_001272003.1:c.1407C= NP_001258932.1:p.Tyr469=
NM_020822.2:c.1542C= NP_065873.2:p.Tyr514=
XM_011518877.1:c.1677C= XP_011517179.1:p.Tyr559=
XM_011518878.1:c.1686C= XP_011517180.1:p.Tyr562=
XM_011518879.1:c.1677C= XP_011517181.1:p.Tyr559=
XM_011518880.1:c.1443C= XP_011517182.1:p.Tyr481=
XM_011518881.1:c.1032C= XP_011517183.1:p.Tyr344=
XM_011518877.3:c.1677C= XP_011517179.1:p.Tyr559=
XM_011518878.3:c.1686C= XP_011517180.1:p.Tyr562=
XM_011518879.3:c.1677C= XP_011517181.1:p.Tyr559=
XM_011518881.3:c.1032C= XP_011517183.1:p.Tyr344=
XM_017014931.1:c.1476C= XP_016870420.1:p.Tyr492=
XM_017014932.1:c.1299C= XP_016870421.1:p.Tyr433=
XM_017014933.1:c.1032C= XP_016870422.1:p.Tyr344=
XM_024447617.1:c.1032C= XP_024303385.1:p.Tyr344=
XM_024447618.1:c.1032C= XP_024303386.1:p.Tyr344=
NM_020822.3:c.1542C= MANE Select NP_065873.2:p.Tyr514=
NM_001272003.2:c.1407C= NP_001258932.1:p.Tyr469=