Canonical Allele Identifier: CA375505947

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138661847T>A (hg19) ; chr9:g.135770001T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770001T>A , CM000671.2:g.135770001T>A	GRCh38
NC_000009.11:g.138661847T>A , CM000671.1:g.138661847T>A	GRCh37
NC_000009.10:g.137801668T>A	NCBI36
NG_033070.1:g.72817T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1565T>A MANE Select	ENSP00000360822.2:p.Ile522Asn
ENST00000674572.1:c.1406T>A	ENSP00000501742.1:p.Ile469Asn
ENST00000675090.1:c.1313T>A	ENSP00000501833.1:p.Ile438Asn
ENST00000675399.1:c.1313T>A	ENSP00000501932.1:p.Ile438Asn
ENST00000676421.1:c.1322T>A	ENSP00000502322.1:p.Ile441Asn
ENST00000263604.5:c.1466T>A	ENSP00000263604.4:p.Ile489Asn
ENST00000371757.6:c.1565T>A	ENSP00000360822.2:p.Ile522Asn
ENST00000460750.5:c.*1175T>A	ENSP00000418777.1:n.*1175T>A
ENST00000486577.6:c.1448T>A	ENSP00000417578.3:p.Ile483Asn
ENST00000487664.5:c.1565T>A	ENSP00000417851.2:p.Ile522Asn
ENST00000488444.6:c.1508T>A	ENSP00000419007.3:p.Ile503Asn
ENST00000490355.6:c.1508T>A	ENSP00000418003.3:p.Ile503Asn
ENST00000490363.3:n.1384T>A
ENST00000491806.6:c.1508T>A	ENSP00000419086.3:p.Ile503Asn
ENST00000628528.2:c.1430T>A	ENSP00000486374.1:p.Ile477Asn
ENST00000630792.2:c.1406T>A	ENSP00000486486.1:p.Ile469Asn
ENST00000631073.2:c.1508T>A	ENSP00000486130.1:p.Ile503Asn
NM_001272003.1:c.1430T>A	NP_001258932.1:p.Ile477Asn
NM_020822.2:c.1565T>A	NP_065873.2:p.Ile522Asn
XM_011518877.1:c.1700T>A	XP_011517179.1:p.Ile567Asn
XM_011518878.1:c.1709T>A	XP_011517180.1:p.Ile570Asn
XM_011518879.1:c.1700T>A	XP_011517181.1:p.Ile567Asn
XM_011518880.1:c.1466T>A	XP_011517182.1:p.Ile489Asn
XM_011518881.1:c.1055T>A	XP_011517183.1:p.Ile352Asn
XM_011518877.3:c.1700T>A	XP_011517179.1:p.Ile567Asn
XM_011518878.3:c.1709T>A	XP_011517180.1:p.Ile570Asn
XM_011518879.3:c.1700T>A	XP_011517181.1:p.Ile567Asn
XM_011518881.3:c.1055T>A	XP_011517183.1:p.Ile352Asn
XM_017014931.1:c.1499T>A	XP_016870420.1:p.Ile500Asn
XM_017014932.1:c.1322T>A	XP_016870421.1:p.Ile441Asn
XM_017014933.1:c.1055T>A	XP_016870422.1:p.Ile352Asn
XM_024447617.1:c.1055T>A	XP_024303385.1:p.Ile352Asn
XM_024447618.1:c.1055T>A	XP_024303386.1:p.Ile352Asn
NM_020822.3:c.1565T>A MANE Select	NP_065873.2:p.Ile522Asn
NM_001272003.2:c.1430T>A	NP_001258932.1:p.Ile477Asn