Canonical Allele Identifier: CA375505858
Gene: KCNT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135769963G>C , CM000671.2:g.135769963G>C GRCh38
NC_000009.11:g.138661809G>C , CM000671.1:g.138661809G>C GRCh37
NC_000009.10:g.137801630G>C NCBI36
NG_033070.1:g.72779G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.1527G>C MANE Select ENSP00000360822.2:p.Glu509Asp
ENST00000674572.1:c.1368G>C ENSP00000501742.1:p.Glu456Asp
ENST00000675090.1:c.1275G>C ENSP00000501833.1:p.Glu425Asp
ENST00000675399.1:c.1275G>C ENSP00000501932.1:p.Glu425Asp
ENST00000676421.1:c.1284G>C ENSP00000502322.1:p.Glu428Asp
ENST00000263604.5:c.1428G>C ENSP00000263604.4:p.Glu476Asp
ENST00000371757.6:c.1527G>C ENSP00000360822.2:p.Glu509Asp
ENST00000460750.5:c.*1137G>C ENSP00000418777.1:n.*1137G>C
ENST00000486577.6:c.1410G>C ENSP00000417578.3:p.Glu470Asp
ENST00000487664.5:c.1527G>C ENSP00000417851.2:p.Glu509Asp
ENST00000488444.6:c.1470G>C ENSP00000419007.3:p.Glu490Asp
ENST00000490355.6:c.1470G>C ENSP00000418003.3:p.Glu490Asp
ENST00000490363.3:n.1346G>C
ENST00000491806.6:c.1470G>C ENSP00000419086.3:p.Glu490Asp
ENST00000628528.2:c.1392G>C ENSP00000486374.1:p.Glu464Asp
ENST00000630792.2:c.1368G>C ENSP00000486486.1:p.Glu456Asp
ENST00000631073.2:c.1470G>C ENSP00000486130.1:p.Glu490Asp
NM_001272003.1:c.1392G>C NP_001258932.1:p.Glu464Asp
NM_020822.2:c.1527G>C NP_065873.2:p.Glu509Asp
XM_011518877.1:c.1662G>C XP_011517179.1:p.Glu554Asp
XM_011518878.1:c.1671G>C XP_011517180.1:p.Glu557Asp
XM_011518879.1:c.1662G>C XP_011517181.1:p.Glu554Asp
XM_011518880.1:c.1428G>C XP_011517182.1:p.Glu476Asp
XM_011518881.1:c.1017G>C XP_011517183.1:p.Glu339Asp
XM_011518877.3:c.1662G>C XP_011517179.1:p.Glu554Asp
XM_011518878.3:c.1671G>C XP_011517180.1:p.Glu557Asp
XM_011518879.3:c.1662G>C XP_011517181.1:p.Glu554Asp
XM_011518881.3:c.1017G>C XP_011517183.1:p.Glu339Asp
XM_017014931.1:c.1461G>C XP_016870420.1:p.Glu487Asp
XM_017014932.1:c.1284G>C XP_016870421.1:p.Glu428Asp
XM_017014933.1:c.1017G>C XP_016870422.1:p.Glu339Asp
XM_024447617.1:c.1017G>C XP_024303385.1:p.Glu339Asp
XM_024447618.1:c.1017G>C XP_024303386.1:p.Glu339Asp
NM_020822.3:c.1527G>C MANE Select NP_065873.2:p.Glu509Asp
NM_001272003.2:c.1392G>C NP_001258932.1:p.Glu464Asp