Canonical Allele Identifier: CA375494756

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138641975A>G (hg19) ; chr9:g.135750129A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135750129A>G , CM000671.2:g.135750129A>G	GRCh38
NC_000009.11:g.138641975A>G , CM000671.1:g.138641975A>G	GRCh37
NC_000009.10:g.137781796A>G	NCBI36
NG_033070.1:g.52945A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.286A>G MANE Select	ENSP00000360822.2:p.Thr96Ala
ENST00000637018.1:n.91A>G
ENST00000638123.1:n.21A>G
ENST00000674572.1:c.127A>G	ENSP00000501742.1:p.Thr43Ala
ENST00000675090.1:c.34A>G	ENSP00000501833.1:p.Thr12Ala
ENST00000675399.1:c.34A>G	ENSP00000501932.1:p.Thr12Ala
ENST00000676421.1:c.34A>G	ENSP00000502322.1:p.Thr12Ala
ENST00000263604.5:c.187A>G	ENSP00000263604.4:p.Thr63Ala
ENST00000371757.6:c.286A>G	ENSP00000360822.2:p.Thr96Ala
ENST00000460750.5:c.286A>G	ENSP00000418777.1:p.Thr96Ala
ENST00000473941.5:c.127A>G	ENSP00000420764.1:p.Thr43Ala
ENST00000486577.6:c.169A>G	ENSP00000417578.3:p.Thr57Ala
ENST00000487664.5:c.286A>G	ENSP00000417851.2:p.Thr96Ala
ENST00000488444.6:c.229A>G	ENSP00000419007.3:p.Thr77Ala
ENST00000490355.6:c.229A>G	ENSP00000418003.3:p.Thr77Ala
ENST00000491806.6:c.229A>G	ENSP00000419086.3:p.Thr77Ala
ENST00000628528.2:c.142A>G	ENSP00000486374.1:p.Thr48Ala
ENST00000630792.2:c.127A>G	ENSP00000486486.1:p.Thr43Ala
ENST00000631073.2:c.229A>G	ENSP00000486130.1:p.Thr77Ala
NM_001272003.1:c.142A>G	NP_001258932.1:p.Thr48Ala
NM_020822.2:c.286A>G	NP_065873.2:p.Thr96Ala
XM_011518877.1:c.421A>G	XP_011517179.1:p.Thr141Ala
XM_011518878.1:c.421A>G	XP_011517180.1:p.Thr141Ala
XM_011518879.1:c.421A>G	XP_011517181.1:p.Thr141Ala
XM_011518880.1:c.187A>G	XP_011517182.1:p.Thr63Ala
XM_011518877.3:c.421A>G	XP_011517179.1:p.Thr141Ala
XM_011518878.3:c.421A>G	XP_011517180.1:p.Thr141Ala
XM_011518879.3:c.421A>G	XP_011517181.1:p.Thr141Ala
XM_017014931.1:c.311A>G	XP_016870420.1:p.His104Arg
XM_017014932.1:c.34A>G	XP_016870421.1:p.Thr12Ala
XM_017014933.1:c.-134A>G	XP_016870422.1:n.-134A>G
XM_024447617.1:c.-234A>G	XP_024303385.1:n.-234A>G
XM_024447618.1:c.-234A>G	XP_024303386.1:n.-234A>G
NM_020822.3:c.286A>G MANE Select	NP_065873.2:p.Thr96Ala
NM_001272003.2:c.142A>G	NP_001258932.1:p.Thr48Ala