Canonical Allele Identifier: CA375501815

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138657591A>T (hg19) ; chr9:g.135765745A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765745A>T , CM000671.2:g.135765745A>T	GRCh38
NC_000009.11:g.138657591A>T , CM000671.1:g.138657591A>T	GRCh37
NC_000009.10:g.137797412A>T	NCBI36
NG_033070.1:g.68561A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1322A>T MANE Select	ENSP00000360822.2:p.Asp441Val
ENST00000636003.1:c.12A>T
ENST00000636995.1:n.49A>T
ENST00000637798.1:n.61A>T
ENST00000674572.1:c.1163A>T	ENSP00000501742.1:p.Asp388Val
ENST00000675090.1:c.1070A>T	ENSP00000501833.1:p.Asp357Val
ENST00000675399.1:c.1070A>T	ENSP00000501932.1:p.Asp357Val
ENST00000676421.1:c.1079A>T	ENSP00000502322.1:p.Asp360Val
ENST00000263604.5:c.1223A>T	ENSP00000263604.4:p.Asp408Val
ENST00000371757.6:c.1322A>T	ENSP00000360822.2:p.Asp441Val
ENST00000460750.5:c.*932A>T	ENSP00000418777.1:n.*932A>T
ENST00000486577.6:c.1205A>T	ENSP00000417578.3:p.Asp402Val
ENST00000487664.5:c.1322A>T	ENSP00000417851.2:p.Asp441Val
ENST00000488444.6:c.1265A>T	ENSP00000419007.3:p.Asp422Val
ENST00000490355.6:c.1265A>T	ENSP00000418003.3:p.Asp422Val
ENST00000490363.3:n.1141A>T
ENST00000491806.6:c.1265A>T	ENSP00000419086.3:p.Asp422Val
ENST00000628528.2:c.1187A>T	ENSP00000486374.1:p.Asp396Val
ENST00000630792.2:c.1163A>T	ENSP00000486486.1:p.Asp388Val
ENST00000631073.2:c.1265A>T	ENSP00000486130.1:p.Asp422Val
NM_001272003.1:c.1187A>T	NP_001258932.1:p.Asp396Val
NM_020822.2:c.1322A>T	NP_065873.2:p.Asp441Val
XM_011518877.1:c.1457A>T	XP_011517179.1:p.Asp486Val
XM_011518878.1:c.1466A>T	XP_011517180.1:p.Asp489Val
XM_011518879.1:c.1457A>T	XP_011517181.1:p.Asp486Val
XM_011518880.1:c.1223A>T	XP_011517182.1:p.Asp408Val
XM_011518881.1:c.812A>T	XP_011517183.1:p.Asp271Val
XM_011518877.3:c.1457A>T	XP_011517179.1:p.Asp486Val
XM_011518878.3:c.1466A>T	XP_011517180.1:p.Asp489Val
XM_011518879.3:c.1457A>T	XP_011517181.1:p.Asp486Val
XM_011518881.3:c.812A>T	XP_011517183.1:p.Asp271Val
XM_017014931.1:c.1256A>T	XP_016870420.1:p.Asp419Val
XM_017014932.1:c.1079A>T	XP_016870421.1:p.Asp360Val
XM_017014933.1:c.812A>T	XP_016870422.1:p.Asp271Val
XM_024447617.1:c.812A>T	XP_024303385.1:p.Asp271Val
XM_024447618.1:c.812A>T	XP_024303386.1:p.Asp271Val
NM_020822.3:c.1322A>T MANE Select	NP_065873.2:p.Asp441Val
NM_001272003.2:c.1187A>T	NP_001258932.1:p.Asp396Val