Canonical Allele Identifier: CA375506004

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138661874C>G (hg19) ; chr9:g.135770028C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770028C>G , CM000671.2:g.135770028C>G	GRCh38
NC_000009.11:g.138661874C>G , CM000671.1:g.138661874C>G	GRCh37
NC_000009.10:g.137801695C>G	NCBI36
NG_033070.1:g.72844C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1592C>G MANE Select	ENSP00000360822.2:p.Thr531Ser
ENST00000674572.1:c.1433C>G	ENSP00000501742.1:p.Thr478Ser
ENST00000675090.1:c.1340C>G	ENSP00000501833.1:p.Thr447Ser
ENST00000675399.1:c.1340C>G	ENSP00000501932.1:p.Thr447Ser
ENST00000676421.1:c.1349C>G	ENSP00000502322.1:p.Thr450Ser
ENST00000263604.5:c.1493C>G	ENSP00000263604.4:p.Thr498Ser
ENST00000371757.6:c.1592C>G	ENSP00000360822.2:p.Thr531Ser
ENST00000460750.5:c.*1202C>G	ENSP00000418777.1:n.*1202C>G
ENST00000486577.6:c.1475C>G	ENSP00000417578.3:p.Thr492Ser
ENST00000487664.5:c.1592C>G	ENSP00000417851.2:p.Thr531Ser
ENST00000488444.6:c.1535C>G	ENSP00000419007.3:p.Thr512Ser
ENST00000490355.6:c.1535C>G	ENSP00000418003.3:p.Thr512Ser
ENST00000490363.3:n.1411C>G
ENST00000491806.6:c.1535C>G	ENSP00000419086.3:p.Thr512Ser
ENST00000628528.2:c.1457C>G	ENSP00000486374.1:p.Thr486Ser
ENST00000630792.2:c.1433C>G	ENSP00000486486.1:p.Thr478Ser
ENST00000631073.2:c.1535C>G	ENSP00000486130.1:p.Thr512Ser
NM_001272003.1:c.1457C>G	NP_001258932.1:p.Thr486Ser
NM_020822.2:c.1592C>G	NP_065873.2:p.Thr531Ser
XM_011518877.1:c.1727C>G	XP_011517179.1:p.Thr576Ser
XM_011518878.1:c.1736C>G	XP_011517180.1:p.Thr579Ser
XM_011518879.1:c.1727C>G	XP_011517181.1:p.Thr576Ser
XM_011518880.1:c.1493C>G	XP_011517182.1:p.Thr498Ser
XM_011518881.1:c.1082C>G	XP_011517183.1:p.Thr361Ser
XM_011518877.3:c.1727C>G	XP_011517179.1:p.Thr576Ser
XM_011518878.3:c.1736C>G	XP_011517180.1:p.Thr579Ser
XM_011518879.3:c.1727C>G	XP_011517181.1:p.Thr576Ser
XM_011518881.3:c.1082C>G	XP_011517183.1:p.Thr361Ser
XM_017014931.1:c.1526C>G	XP_016870420.1:p.Thr509Ser
XM_017014932.1:c.1349C>G	XP_016870421.1:p.Thr450Ser
XM_017014933.1:c.1082C>G	XP_016870422.1:p.Thr361Ser
XM_024447617.1:c.1082C>G	XP_024303385.1:p.Thr361Ser
XM_024447618.1:c.1082C>G	XP_024303386.1:p.Thr361Ser
NM_020822.3:c.1592C>G MANE Select	NP_065873.2:p.Thr531Ser
NM_001272003.2:c.1457C>G	NP_001258932.1:p.Thr486Ser